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Indian Journal of Human Genetics

ISSN: 0971--6866
Publisher: Medknow Publications on behalf of Indian Society of Human Genetics


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Rett syndrome molecular diagnosis and implications in genetic counseling

Author(s): Noruzinia M | Akbari M | Ghofrani M | Sheikhha H
Volume: 13
Issue: 3
Year: 2007
Emergence of an unrelated highly aberrant clone in an AML patient at relapse four months after peripheral blood stem cell transplantation

Author(s): Kadam Pratibha | Jain Hemani | Parikh Purvish | Saikia Tapan | Agarwal Sandhya | Ambulkar Indu
Volume: 13
Issue: 3
Year: 2007
Possible risk factors for Down syndrome and sex chromosomal aneuploidy in Mysore, South India

Author(s): Malini Suttur | Ramachandra Nallur
Volume: 13
Issue: 3
Year: 2007
PvuII polymorphism of estrogen receptor-α gene in breast cancer

Author(s): Surekha D | Vishnupriya S | Rao D | Sailaja K | Raghunadharao D
Volume: 13
Issue: 3
Year: 2007
DNA profiling: Social, legal, or biological parentage

Author(s): Sharma A
Volume: 13
Issue: 3
Year: 2007
Coagulation disorders seen through the window of molecular biology

Author(s): Ghosh Kanjaksha
Volume: 13
Issue: 3
Year: 2007
Role of intrauterine Rubella infection in the causation of congenital deafness

Author(s): Reddy MVV | Bindu Hema | Reddy P | Rani Usha
Volume: 12
Issue: 3
Year: 2006
Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases

Author(s): Rao Babu | Kerketta Lily | Korgaonkar Seema | Ghosh Kanjaksha
Volume: 12
Issue: 3
Year: 2006
Superoxide dismutase phenotypes in duodenal ulcers: A genetic marker?

Author(s): Sulekha S | Madhavi J | Venkateshwari A | Yasmeen S | Pratibha N
Volume: 12
Issue: 3
Year: 2006
Molecular tissue typing in renal transplantation: Initial experience from a tertiary care Naval Hospital

Author(s): Mishra Mahendra | Mani Haresh | Saxena Vinod | Gupta Mahendra
Volume: 12
Issue: 3
Year: 2006
Genetic heterogeneity in duodenal ulceration

Author(s): Venkateshwari A | Vidyasagar A | Pratibha N
Volume: 12
Issue: 3
Year: 2006
Lack of association of Endoglin insertion polymorphism in intracranial aneurysm in South Indian population

Author(s): Koshy Linda | Easwer H | Bhattacharya R | Banerjee Moinak
Volume: 12
Issue: 3
Year: 2006
Association of SP-D, MBL and I-NOS genetic variants with pulmonary tuberculosis

Author(s): Vaid Mudit | Kaur Savneet | Taruna Madan | Singh Hari | Gupta Vijay | Murthy KJR | Sarma Puranam
Volume: 12
Issue: 3
Year: 2006
Fluctuating asymmetry in dermatoglyphics of non-insulin-dependent diabetes mellitus in Bangalore-based population

Author(s): Ravindranath R | Joseph A | Bosco S | Rajangam S | Balasubramanyam V
Volume: 11
Issue: 3
Year: 2005
Red cell enzyme and serum protein polymorphisms (ACP1, PGM1, GLO1, ESD, HP, PI) in Turkish population

Author(s): Donbak L | Csete C | Salacin S | Varga T
Volume: 11
Issue: 3
Year: 2005
Modes of genetic transmission of dyslexia in south Indian families

Author(s): Saviour P | Ramachandra N
Volume: 11
Issue: 3
Year: 2005
Genomic and expression array profiling of chromosome 20q amplicon in human colon cancer cells

Author(s): Carter Jennifer | Jin Li | Sen Subrata
Volume: 11
Issue: 3
Year: 2005
Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?

Author(s): Hamzi Khalil | Itto Afaf | Nassereddine Sanaa | Nadifi Sellama
Volume: 16
Issue: 3
Year: 2010
Molecular analysis of human leukocyte antigen class I and class II allele frequencies and haplotype distribution in Pakistani population

Author(s): Moatter T | Aban M | Tabassum S | Shaikh U | Pervez S
Volume: 16
Issue: 3
Year: 2010
Genetic assessment of serological and biochemical markers in Bharia tribe of Chhindwara district of Madhya Pradesh

Author(s): Chaudhary Ruchira | Sharma Gunjan
Volume: 16
Issue: 3
Year: 2010
Bone age is the best predictor of growth response to recombinant human growth hormone in Turner′s syndrome

Author(s): Ismail Nagwa | Metwaly Nermeen | El-Moguy Fatma | Hafez Mona | Abd El Dayem Soha | Farid Tarek
Volume: 16
Issue: 3
Year: 2010
Pharmacogenomics of pediatric asthma

Author(s): Gupta Sarika | Awasthi Shally
Volume: 16
Issue: 3
Year: 2010
Natural selection among Kinnaura of the Himalayan highland: A comparative analysis with other Indian and Himalayan populations

Author(s): Gautam Rajesh | Kapoor Anup | Kshatriya G
Volume: 15
Issue: 3
Year: 2009
GITR expression on T-cell receptor-stimulated human CD8+ T cell in a JNK-dependent pathway

Author(s): Chattopadhyay Subhasis | Chakraborty Nitya
Volume: 15
Issue: 3
Year: 2009
Microsatellite diversity among the primitive tribes of India

Author(s): Mukherjee Malay | Tripathy V | Colah R | Solanki P | Ghosh K | Reddy B | Mohanty D
Volume: 15
Issue: 3
Year: 2009
Frequency of fokI and taqI polymorphism of vitamin D receptor gene in Indian population and its association with 25-hydroxyvitamin D levels

Author(s): Bhanushali Aparna | Lajpal Namrata | Kulkarni Smita | Chavan Sandeep | Bagadi Sarita | Das Bibhu
Volume: 15
Issue: 3
Year: 2009
APO-1/Fas gene: Structural and functional characteristics in systemic lupus erythematosus and other autoimmune diseases

Author(s): Singh Richa | Pradhan Vandana | Patwardhan Manisha | Ghosh K
Volume: 15
Issue: 3
Year: 2009
Bloom′s syndrome in a 12-year-old Iranian girl

Author(s): Tayebi Naeimeh | Khodaei Hossain
Volume: 14
Issue: 3
Year: 2008
The CTLA4 -819 C/T and +49 A/G dimorphisms are associated with Type 1 diabetes in Egyptian children

Author(s): Saleh Hatem | Rohowsky Nestor | Leski Michael
Volume: 14
Issue: 3
Year: 2008
Standardization of PCR-RFLP analysis of nsSNP rs1468384 of NPC1L1 gene

Author(s): Balgir Praveen | Khanna Divya | Kaur Gurlovleen
Volume: 14
Issue: 3
Year: 2008
Fc gamma receptor polymorphisms in systemic lupus erythematosus and their correlation with the clinical severity of the disease

Author(s): Pradhan Vandana | Patwardhan Manisha | Ghosh K
Volume: 14
Issue: 3
Year: 2008
Oculo-facio-cardio-dental syndrome in a girl and her mother

Author(s): Rudrappa Sudha | Kumar Rajendra | Kumar G
Volume: 16
Issue: 3
Year: 2010
A rare case of congenital heart disease with ambiguous genitalia

Author(s): Lingaiah Kusuma | Parshwanath Bharath | Mysore Savitha | Krishnamurthy Balasundaram | Ramachandra Nallur
Volume: 16
Issue: 3
Year: 2010
A Sri Lankan child with 49,XXXXY syndrome

Author(s): Dissanayake Vajira | Bandarage Palinda | Pedurupillay Christeen | Jayasekara Rohan
Volume: 16
Issue: 3
Year: 2010
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

Author(s): Mukherjee Malay | Nadkarni Anita | Gorakshakar Ajit | Ghosh Kanjaksha | Mohanty Dipika | Colah Roshan
Volume: 16
Issue: 3
Year: 2010
Complexities and similarities of HLA antigen distribution in Asian subcontinent

Author(s): Shankarkumar U
Volume: 16
Issue: 3
Year: 2010
Ectrodactyly/split hand feet malformation

Author(s): Jindal Geetanjali | Parmar Veena | Gupta Vipul
Volume: 15
Issue: 3
Year: 2009
A new recurring chromosome 13 abnormality in two older patients with de novo acute myeloid leukemia: An Indian experience

Author(s): Trivedi P | Patel P | Brahmbhatt M | Patel B | Gajjar S | Dalal E | Shukla S | Shah P | Bakshi S
Volume: 15
Issue: 3
Year: 2009
Genetic studies in children with intellectual disability and autistic spectrum of disorders

Author(s): Balasubramanian Bhanumathi | Bhatt Chetna | Goyel Neelam
Volume: 15
Issue: 3
Year: 2009
Mitochondrial DNA mutations and male infertility

Author(s): Kumar D | Sangeetha N
Volume: 15
Issue: 3
Year: 2009
Genetics of autism and mental retardation: A spoonful from the sea!

Author(s): Ghosh Kanjaksha | Gorakshakar Ajit
Volume: 15
Issue: 3
Year: 2009
The moroccan human mutation database

Author(s): Ratbi Ilham | Gati Alae-eddine | Sefiani Abdelaziz
Volume: 14
Issue: 3
Year: 2008
National and ethnic human mutation database: A need of the day

Author(s): Gorakshakar A | Ghosh K
Volume: 14
Issue: 3
Year: 2008
Translocation t(2;14)(p13;q32) in a case of Ph+ acute lymphoblastic leukemia

Author(s): Kerketta Lily | Vundinti Babu | Ghosh Kanjaksha
Volume: 13
Issue: 3
Year: 2007
Mowat-Wilson syndrome in a Moroccan consanguineous family

Author(s): Ratbi Ilham | Elalaoui Chafai | Dastot-Le Moal | Goossens Michel | Giurgea Irina | Sefiani Abdelaziz
Volume: 13
Issue: 3
Year: 2007
Chromosome 12;15 rearrangements in patients with recurrent miscarriage

Author(s): Nair S | Mukundan G | Paul B | Ramachandran L | Gopinathan K | Joseph Sajayan
Volume: 12
Issue: 3
Year: 2006
Facio-auricular vertebral syndrome-a case report

Author(s): Reddy M | Reddy P | Usha Rani P | Hema Bindu L
Volume: 11
Issue: 3
Year: 2005
Congenital malformations at birth in Central India: A rural medical college hospital based data

Author(s): Taksande Amar | Vilhekar Krishna | Chaturvedi Pushpa | Jain Manish
Volume: 16
Issue: 3
Year: 2010
Iranian human genome project: Overview of a research process among Iranian ethnicities

Author(s): Banihashemi Kambiz
Volume: 15
Issue: 3
Year: 2009
Allelic variants of DYX1C1 are not associated with dyslexia in India

Author(s): Saviour Pushpa | Kumar Satish | Kiran U | Ravuri Rajasekhara | Rao V | Ramachandra Nallur
Volume: 14
Issue: 3
Year: 2008
Adenocarcinoma of the colon and rectum in the Kashmiri population

Author(s): Sameer A | Chowdhri Nissar | Siddiqi Mushtaq
Volume: 15
Issue: 3
Year: 2009
Bombay phenotype in Orissa: What could we make out of it?

Author(s): Ghosh Kanjaksha | Vasantha K
Volume: 13
Issue: 3
Year: 2007
11th International Congress on Human Genetics 2006

Author(s): Mukherjee M
Volume: 12
Issue: 3
Year: 2006
The case for dedicated sickle cell centres

Author(s): Serjeant Graham
Volume: 12
Issue: 3
Year: 2006
TRISOMY 18 in a 50-year-old female

Author(s): Bhanumathi B | Goyel Neelam | Mishra Z
Volume: 12
Issue: 3
Year: 2006
ABCD syndrome revisited

Author(s): Kothari Paras | Sarda Dinesh | Shankar Gauri | Kulkarni Bharati
Volume: 12
Issue: 3
Year: 2006
Mobile phone users-time to sit up and listen

Author(s): Ghosh Malay
Volume: 11
Issue: 3
Year: 2005
Hemoglobin sickle D Punjab-a case report

Author(s): Mukherjee M | Surve R | Gangakhedkar R | Mohanty D | Colah R
Volume: 11
Issue: 3
Year: 2005
The treatment of Gaucher disease in countries with limited health care resources

Author(s): Beutler Ernest
Volume: 11
Issue: 3
Year: 2005
"Jack of all trades"-editors of medical journals in India

Author(s): Ghosh K
Volume: 11
Issue: 3
Year: 2005
Plasma Lipoprotein (a) levels in patients with untreated essential hypertension

Author(s): Bhavani B | Padma T | Sastry BKS | Reddy N
Volume: 9
Issue: 2
Year: 2003
Connexin 26 and autosomal recessive non-syndromic hearing loss

Author(s): Mukherjee Monisha | Phadke S | Mittal Balraj
Volume: 9
Issue: 2
Year: 2003
Detection of Y STR markers of male fetal dna in maternal circulation

Author(s): Nair Seema | Peter Sam | Pillay V | Remya U | Krishnaprasad R | Rajammal B
Volume: 13
Issue: 2
Year: 2007
Distribution profile of paraoxonase phenotypes among the Gujaratis

Author(s): Patel A | Pal R | Dewan A
Volume: 13
Issue: 2
Year: 2007
Human sex ratio at birth in South West Nigeria

Author(s): Azeez M | Akinboro A | Bakare A
Volume: 13
Issue: 2
Year: 2007
Dopamine receptor D4 exon 3 variable number of tandem repeat polymorphism: Distribution in eastern Indian population

Author(s): Bhaduri Nipa | Das Manali | Das Aneek | Mukhopadhyay Kanchan
Volume: 13
Issue: 2
Year: 2007
Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases

Author(s): Annapurna S | Reena T | Nallari Pratibha | Calambur Narasimhan
Volume: 13
Issue: 2
Year: 2007
Complement receptor 1 and the molecular pathogenesis of malaria

Author(s): Gandhi Monika
Volume: 13
Issue: 2
Year: 2007
Detection of L1 (CAM) mutations in X-linked mental retardation: A study from Andhra Pradesh, India

Author(s): Jharna P | Hemabindu L | Siva Prasad S | Swarna M | Sujatha M | Rani P | Reddy P
Volume: 12
Issue: 2
Year: 2006
Fluctuating asymmetry in dermatoglyphics of carcinoma of breast

Author(s): Natekar Prashant | DeSouza Fatima
Volume: 12
Issue: 2
Year: 2006
Association of apolipoprotein E (RFLP) polymorphism with myopia

Author(s): Himabindu P | Vishnupriya S | Padma T | Rao Vittal | Shravan Kumar K | Bhavani M | Reddy Ramakrishna
Volume: 12
Issue: 2
Year: 2006
Y chromosome microdeletions in Turkish infertile men

Author(s): Zamani Ayse | Kutlu Ruhusen | Durakbasi-Dursun H | Gorkemli Huseyin | Acar Aynur
Volume: 12
Issue: 2
Year: 2006
Clinical relevance of alternative splicing

Author(s): Ravindra T | Lakshmi N | Chaitanya K | Surender V | Ahuja Y
Volume: 12
Issue: 2
Year: 2006
Molecular characterization of mutations causing β -thalassemia in Faisalabad Pakistan using the amplification refractory mutation system (ARMS-PCR)

Author(s): Baig Shahid | Rabbi F | Hameed U | Qureshi J | Mahmood Z | Bokhari S | Kiani A | Hassan H | Baig J | Azhar A | Zaman T
Volume: 11
Issue: 2
Year: 2005
Detection of two rare β -thalassemia mutations [-90 (C ® T) and CD 26 (C ®T)] among Indians

Author(s): Gorakshakar A | Phanasgaonkar S | Colah R | Mohanty D
Volume: 11
Issue: 2
Year: 2005
Consanguinity and chromosomal abnormality

Author(s): Amudha S | Aruna N | Rajangam S
Volume: 11
Issue: 2
Year: 2005
Isolated cell translocations: Are they significant?

Author(s): Devi R | Sayee R
Volume: 11
Issue: 2
Year: 2005
Genetic damage in mobile phone users: some preliminary findings

Author(s): Gandhi Gursatej | Anita
Volume: 11
Issue: 2
Year: 2005
Cytogenetic causes for recurrent spontaneous abortions - An experience of 742 couples (1484 cases)

Author(s): Dubey S | Chowdhury M | Prahlad B | Kumar V | Mathur R | Hamilton S | Kabra M | Menon P | Verma I
Volume: 11
Issue: 2
Year: 2005
The frequency of GSTT1 null genotype in Turkish population and lung cancer risk

Author(s): Demir A | Altin S | Demir I | Koksal V | Cetincelik U | Dincer S
Volume: 11
Issue: 2
Year: 2005
Molecular characterization of mutations causing β -thalassemia in Faisalabad Pakistan using the amplification refractory mutation system (ARMS-PCR)

Author(s): Baig Shahid | Rabbi F | Hameed U | Qureshi J | Mahmood Z | Bokhari S | Kiani A | Hassan H | Baig J | Azhar A | Zaman T
Volume: 11
Issue: 2
Year: 2005
Detection of two rare β -thalassemia mutations [-90 (C ® T) and CD 26 (C ®T)] among Indians

Author(s): Gorakshakar A | Phanasgaonkar S | Colah R | Mohanty D
Volume: 11
Issue: 2
Year: 2005
Contribution of genomics, proteomics, and single-nucleotide polymorphism in toxicology research and Indian scenario

Author(s): Patel S | Parmar D | Gupta Y | Singh M
Volume: 11
Issue: 2
Year: 2005
Null association between ACE gene I/D polymorphism and diabetic nephropathy among multiethnic Malaysian subjects

Author(s): Jayapalan Jaime | Muniandy Sekaran | Chan Siew
Volume: 16
Issue: 2
Year: 2010
Association of polymorphisms in leptin receptor gene with obesity and type 2 diabetes in the local population of Coimbatore

Author(s): Murugesan Devi | Arunachalam Thirunavukkarasu | Ramamurthy Viraragavan | Subramanian Selvi
Volume: 16
Issue: 2
Year: 2010
Drugs impact on CYP-450 enzyme family: A pharmacogenetical study of response variation

Author(s): Kalra Kapil | Jarmal Garima | Mishra Neeti
Volume: 15
Issue: 2
Year: 2009
Polymorphic analysis of MHClinked Heat Shock Protein 70 genes: Their susceptibility and prognostic implication in Kangri cancer cases of Kashmiri population

Author(s): Rehman Shakeel | Sameer A | Zahoor Lubna | Syeed Nidda | Nanda Mahoor | Hafiz Adil | Shah Zaffar | Siddiqi Mushtaq
Volume: 15
Issue: 2
Year: 2009
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridization

Author(s): Chetta M | Drmanac A | Santacroce R | Grandone E | Surrey S | Fortina P | Margaglione M
Volume: 14
Issue: 2
Year: 2008
Association of β2-adrenergic receptor and insulin receptor substrate-1 polymorphisms with obesity in a Northern Indian population

Author(s): Srivastava Neena | Achyut B | Prakash Jai | Agarwal C | Pant D | Mittal Balraj
Volume: 14
Issue: 2
Year: 2008
Frequency of twinning in southwest Nigeria

Author(s): Akinboro A | Azeez M | Bakare A
Volume: 14
Issue: 2
Year: 2008
t-plasminogen activator inhibitor-1 polymorphism in idiopathic pulmonary arterial hypertension

Author(s): Katta Sujana | Vadapalli Shivani | Sastry BKS | Nallari Pratibha
Volume: 14
Issue: 2
Year: 2008
Phenotypic correlations in a patient with ring chromosome 22

Author(s): Demirhan Osman | Tunç Erdal
Volume: 16
Issue: 2
Year: 2010
Triploidy in a fetus following amniocentesis referred for maternal serum screening test at second trimester

Author(s): Bagherizadeh E | Oveisi M | Hadipour Z | Saremi A | Shafaghati Y | Behjati F
Volume: 16
Issue: 2
Year: 2010
Opportunity for natural selection among some selected population groups of Northeast India

Author(s): Das Farida | Sikdar Mithun
Volume: 16
Issue: 2
Year: 2010
Rare association of turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex

Author(s): Suttur Malini | Mysore Savitha | Krishnamurthy Balasundaram | Nallur Ramachandra
Volume: 15
Issue: 2
Year: 2009
Linkage analysis of three families with arrythmogenic right ventricular cardiomyopathy in India

Author(s): Dokuparthi Maithili | Pamuru Pranathi | Oruganti Sai | Calambur Narsimhan | Nallari Pratibha
Volume: 15
Issue: 2
Year: 2009
High risk of essential hypertension in males with intron 4 VNTR polymorphism of eNOS gene

Author(s): Patkar Sushma | Charita B | Ramesh C | Padma T
Volume: 15
Issue: 2
Year: 2009
Hereditary multiple exostoses and schizophrenia

Author(s): Gomez-Bernal German
Volume: 14
Issue: 2
Year: 2008
Selection intensity among Kshatriyas an endogamous population of Andhra Pradesh

Author(s): Dharani Priya | P Veerraju | Rao T
Volume: 9
Issue: 2
Year: 2003
Risk of Down syndrome conferred by MTHFR C677T polymorphism: Ethnic variations

Author(s): Dutta Samikshan | Das Aneek | Mukhopadhyay Kanchan
Volume: 13
Issue: 2
Year: 2007
Camptodactyly in Sotos syndrome

Author(s): Danda S | Mathew M | Bain S | Palnok S
Volume: 13
Issue: 2
Year: 2007
Kenny-Caffey syndrome

Author(s): Agarwal Indira | Danda Sumita | Scott Julius | Kumar T | Mammen Thomas
Volume: 12
Issue: 2
Year: 2006
Lissencephaly child showing FISH negative and mutation in DCX gene with normal parental genetic makeup

Author(s): Gupta Bhushan | Verma Sohani | Raina V | Iravathy Goud
Volume: 12
Issue: 2
Year: 2006
AML-M2 with der(18)t(1;18)(q2?;p11.3) in addition to t(8;21) and del(9q)

Author(s): Bakshi Sonal | Roy Shambhu | Trivedi Pina | Brahmbhatt Manisha | Rawal Shwetal | Kakadia Purvi | Bhatt Samarth
Volume: 10
Issue: 2
Year: 2004
HLA Chimerism in allogenic haplo-identical peripheral blood stem cell transplant

Author(s): Chhaya Sonal | Sawant Rajesh | Rajadhyaksha Sunil
Volume: 10
Issue: 2
Year: 2004
Mitotic index in down syndrome - Is it an indicator of immunological status

Author(s): Ranganath Priya | Suresh Geetha | Subramaniam Amudha | Rajangam Sayee
Volume: 10
Issue: 2
Year: 2004
Physical growth of children with sickle cell disease

Author(s): Mukherjee Malay | Gangakhedkar R
Volume: 10
Issue: 2
Year: 2004
Lack of association of NAT2 (N-acetyl transferase 2) gene polymorphism with atopic asthma in Turkish subjects

Author(s): Ceyhan Berrin Bagci | Burgos Ariadna | Palmer Lyle | Drazen Jeffrey
Volume: 10
Issue: 2
Year: 2004
Study of families of nonsyndromic hearing impairment segregating with mutations in Cx26 gene

Author(s): Ramchander P | Nandur V | Dwarakanath K | Vishnupriya S | Padma T
Volume: 10
Issue: 2
Year: 2004
Family based analysis of quantitative changes of erythrocyte membrane proteins in essential hypertension

Author(s): Ivanov Vladimir | Polonikov Alexey | Emeliyanova Oksana | Solodilova Mariya | Mandrik Irina
Volume: 10
Issue: 2
Year: 2004
Molecular analysis of the (CAG)N repeat causing Huntington′s disease in 34 Iranian families

Author(s): Hormozian F | Houshmand Massoud | Sanati M | Ghiasvand R | Banoie M
Volume: 10
Issue: 2
Year: 2004
The diagnostic potential of maternal plasma in detecting fetal diseases by DNA test

Author(s): Saha Biswajit
Volume: 10
Issue: 2
Year: 2004
Trisomy 8p (p11.2-pter) due to maternal translocation t(8;13)(p11;p12) in a child with dysmorphic features

Author(s): Mahjoubi F | Totian S | Kareeme S | Shafegatee Y
Volume: 11
Issue: 2
Year: 2005
Placental chimerism in early human pregnancy

Author(s): Ashutosh Halder
Volume: 11
Issue: 2
Year: 2005
Investigation of chromosomal aberrations in Egyptian hepatocellular carcinoma patients by fluorescence in situ hybridization

Author(s): Aly Magdy | Bahnassy Abeer | Abdel-Rahman Zekri
Volume: 16
Issue: 2
Year: 2010
Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy

Author(s): Tanjore Reena | RangaRaju Advithi | Vadapalli Shivani | Remersu Sushant | Narsimhan Calambur | Nallari Pratibha
Volume: 16
Issue: 2
Year: 2010
Haplotype diversity and linkage disequilibrium at the DRD2 locus among the tribes of western and southern regions of India

Author(s): Aggarwal Aastha | Gauniyal Mansi | Pattanayak Ipsa | Kshatriya Gautam
Volume: 16
Issue: 2
Year: 2010
Genetics in public health: Rarely explored

Author(s): Aswini Y | Varun S
Volume: 16
Issue: 2
Year: 2010
MTHFR Gene variants C677T, A1298C and association with Down syndrome: A case-control study from South India

Author(s): Cyril Cyrus | Rai Padmalatha | Chandra N | Gopinath P | Satyamoorthy K
Volume: 15
Issue: 2
Year: 2009
Distal arthrogryposis syndrome

Author(s): Kulkarni K | Panigrahi I | Ray M | Marwaha R
Volume: 14
Issue: 2
Year: 2008
Significance of t (8: 14) in CLL?

Author(s): Lakshmaiah K | Tejinder S | Kumari Prasanna | Gowri Mangala | Satheesh C | Lokanatha D | Jacob Abraham
Volume: 16
Issue: 2
Year: 2010
Sickle cell hemoglobinopathies in district Bhopal

Author(s): Dangi C. B. S. | Sajid M | Sawke G | Ambhore J
Volume: 16
Issue: 2
Year: 2010
Integration of modern genetic knowledge and technology into public health in India

Author(s): Ghosh Kanjaksha | Gorakshakar Ajit
Volume: 16
Issue: 2
Year: 2010
Down′s syndrome and cardiac tamponade with pulmonary tuberculosis in adults

Author(s): Verma S | Sodhi R
Volume: 15
Issue: 2
Year: 2009
In vitro up-regulation of expression of GITR on human CD8 + cells

Author(s): Thanavala Yasmin
Volume: 15
Issue: 2
Year: 2009
Falciparum malaria selected while HIV-1 slaughtered

Author(s): Ghosh Kanjaksha | Shetty Shrimati | Mota Leenam
Volume: 14
Issue: 2
Year: 2008
A plethora of techniques to detect mutations: Which one to choose?

Author(s): Ghosh K | Shetty S
Volume: 14
Issue: 2
Year: 2008
The Fourth European Cytogenetics Conference, Italy Sept. 2003: A report

Author(s): Madon Prochi
Volume: 9
Issue: 2
Year: 2003
Advances in Genetics: A new direction and distinct medical voice

Author(s): Mohanty Dipika
Volume: 9
Issue: 2
Year: 2003
Genetically predisposed, life style and occurrence of metastatic cancer

Author(s): Chakraborty Nitya
Volume: 13
Issue: 2
Year: 2007
Ocular abnormalities in nail patella syndrome

Author(s): Raja Vignesh | Sandanshiv Pravin | Neugebauer Mark | Sweeney Elizabeth | McIntosh Iain
Volume: 12
Issue: 2
Year: 2006
Tumor-associated antigen and antigen-presenting cells based vaccine therapy for cancer

Author(s): Chakraborty Nitya
Volume: 12
Issue: 2
Year: 2006
Is this cystic fibrosis?

Author(s): Sehgal Arvind
Volume: 10
Issue: 2
Year: 2004
Chromosomal variants and genetic diseases

Author(s): Rao V | Ghosh K
Volume: 11
Issue: 2
Year: 2005
A case of acute myeloid leukemia-M2 with trisomy 4 in addition to t(8;21)

Author(s): Trivedi P | Patel P | Brahmbhatt M | Patel B | Gajjar S | Iyer R | Parikh E | Shukla S | Shah P | Bakshi S
Volume: 14
Issue: 1
Year: 2008
A386G transition in DAZL gene is not associated with spermatogenic failure in Tamil Nadu, South India

Author(s): Poongothai J | Gopenath T | Manonayaki S
Volume: 14
Issue: 1
Year: 2008
Can novel Apo A-I polymorphisms be responsible for low HDL in South Asian immigrants?

Author(s): Dodani Sunita | Dong Yanbin | Zhu Haidong | George Varghese
Volume: 14
Issue: 1
Year: 2008
A cytogenetic study of couples with recurrent spontaneous abortions and infertile patients with recurrent IVF/ICSI failure

Author(s): Mozdarani Hossein | Meybodi Anahita | Zari-Moradi Shabnam
Volume: 14
Issue: 1
Year: 2008
Alternate strategies for carrier detection and antenatal diagnosis in haemophilias in developing countries

Author(s): Shetty Shrimati | Ghosh Kanjaksha | Mohanty Dipika
Volume: 9
Issue: 1
Year: 2003
Spermatogenic alterations in men with high testiculo epididymal temperatures

Author(s): Dada Rima | Gupta N | Kucheria K
Volume: 8
Issue: 1
Year: 2002
Image analysis system and its use in cytogenetic analysis

Author(s): Ahmad Md. Equebal | Kucheria Kiran
Volume: 8
Issue: 1
Year: 2002
Detection of human aneuploidies in prenatal and postnatal diagnosis using molecular cytogenetics

Author(s): Kucheria Kiran | Jobanputra Vaidehi | Talwar Rashmi | Ahmed M | Dada Rima | Sivakumaran T
Volume: 8
Issue: 1
Year: 2002
Evolution of phenylthiocarbamide taster trait in Mysore, South India

Author(s): Malini Suttur | Ramegowda Smitha | Ramachandra Nallur
Volume: 13
Issue: 1
Year: 2007
Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran

Author(s): Fakher Rahim | Bijan Kaeikhaei | Taghi Akbari
Volume: 13
Issue: 1
Year: 2007
Epidemiology and genetics of hypertrophic cardiomyopathy

Author(s): Tanjore Reena | Thakkar Bhavesh | Sikindlapuram Annapurna | Narasimhan Calambur | Kerkar Prafulla | Vajjha Haragopal | Nallari Pratibha
Volume: 12
Issue: 1
Year: 2006
Fragile X screening for FRAXA and FRAXE mutations using PCR based studies: Results of a five year study

Author(s): Chowdhury Madhumita | Kabra Madhulika | Sharma Deepti | Singh Deepika | Dabral Anjali | Thelma B | Kalra Veena
Volume: 12
Issue: 1
Year: 2006
Down syndrome child with 48,XXY,+21 karyotype

Author(s): Cyrus Cyril | Chandra N | Jegatheesan T | Chandralekha K | Ramesh A | Gopinath P | Marimuthu K
Volume: 11
Issue: 1
Year: 2005
Nucleolar organising region evaluation using new NOR FISH probe

Author(s): Rao Babu | Ghosh K | Mohanty D
Volume: 11
Issue: 1
Year: 2005
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India

Author(s): Madan Nishi | Sharma Satendra | Sood S | Colah Roshan | Bhatia H
Volume: 16
Issue: 1
Year: 2010
Gly460Trp polymorphism of the ADD1 gene and essential hypertension in an Indian population: A meta-analysis on hypertension risk

Author(s): Ramu P | Umamaheswaran G | Shewade D | Swaminathan R | Balachander J | Adithan C
Volume: 16
Issue: 1
Year: 2010
Antiplatelet antibodies in cases of Glanzmann′s thrombasthenia with and without a history of multiple platelet transfusion

Author(s): Ghosh Kanjaksha | Kulkarni B | Shetty S | Nair S
Volume: 15
Issue: 1
Year: 2009
Chromosomal instability in the lymphocytes of breast cancer patients

Author(s): Harsimran Kaur | Kaur Monga | Nitika Setia | Meena Sudan | Uppal M | Yamini | Batra A. P. S. | Vasudha Sambyal
Volume: 15
Issue: 1
Year: 2009
Ataxia telangiectasia: Family management

Author(s): Seshachalam Arun | Cyriac Sanju | Reddy Neelesh | Gnana Sagar
Volume: 16
Issue: 1
Year: 2010
Dandy-Walker malformation: An incidental finding

Author(s): Tadakamadla Jyothi | Kumar Santhosh | Mamatha G
Volume: 16
Issue: 1
Year: 2010
Autism and X-linked hypophosphatemia: A possible association?

Author(s): Joel Vermeersch | Hans Hellemans | Dirk Deboutte
Volume: 16
Issue: 1
Year: 2010
Dominant inheritance and intra-familial variations in the association of Sturge-Weber and Klippel-Trenaunay-Weber syndromes

Author(s): Pereira de Godoy Jose | Fett-Conte Agnes
Volume: 16
Issue: 1
Year: 2010
Child with Mongolian spots and dysostosis multiplex

Author(s): Kulkarni Ketan | Murthy Srinivasa | Panigrahi Inusha
Volume: 15
Issue: 1
Year: 2009
Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran

Author(s): Galehdari Hamid | Foroughmand Ali | Soorki Maryam | Mohammadian Gholamreza
Volume: 15
Issue: 1
Year: 2009
Chromosomal instability and cancer: An insight into the rhythm of life

Author(s): Vundinti Babu | Ghosh Kanjaksha
Volume: 15
Issue: 1
Year: 2009
Cornelia de lange syndrome

Author(s): Tayebi Naeimeh
Volume: 14
Issue: 1
Year: 2008
Reactivation of inactive X chromosome in buccal smear of carcinoma of breast

Author(s): Natekar Prashant | DeSouza Fatima
Volume: 14
Issue: 1
Year: 2008
Pairwise MtDNA-HVRII sequence differences and geographic maternal distances among Korku, an Austro-Asiatic tribe in Central India

Author(s): Rao Raghavendra | Thangaraj Kumarasamy | Reddy Alla | Sridhar V | Singh Lalji
Volume: 9
Issue: 1
Year: 2003
Serum Adenosine deaminase activity and C-reactive protein levels in unstable angina

Author(s): Rani Surekha | Rao Dayasagar | M Shiva Prakash | A Jyothy
Volume: 9
Issue: 1
Year: 2003
Blood group and serum protein polymorphisms in turpu kapu population of vizianagaram district, Andhra Pradesh

Author(s): V Komal Madhavi | M Ramesh | Rao T | P Veerraju
Volume: 8
Issue: 1
Year: 2002
Study of some genetic markers in sishta karanam population, Andhra Pradesh, India

Author(s): Naidu V | M Ramesh | Rao T | Veerraju P
Volume: 8
Issue: 1
Year: 2002
Chronic myeloid leukemia: Cytogenetics and molecular genetics

Author(s): Amare Pratibha
Volume: 8
Issue: 1
Year: 2002
Missense mutation G296S in GATA4 is not responsible for cardiac septal defects

Author(s): Ramegowda Smitha | Kumar Arun | Savitha Mysore | Krishnamurthy Balasundaram | Doddaiah Narayanappa | Ramachandra Nallur
Volume: 13
Issue: 1
Year: 2007
Impact of pericentric inversion of Chromosome 9 [inv (9) (p11q12)] on infertility

Author(s): Mozdarani Hossein | Meybodi Anahita | Karimi Hamideh
Volume: 13
Issue: 1
Year: 2007
Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3)

Author(s): Vundinti Babu Rao | Kerketta Lily | Korgaonkar Seema | Ghosh Kanjaksha
Volume: 13
Issue: 1
Year: 2007
CGA codons multiplex PCR in rapid diagnosis of retinoblastoma

Author(s): Mamatha Gandra | Joseph Biju | Shanmugam Mahesh | Kumaramanickavel Govindasamy
Volume: 12
Issue: 1
Year: 2006
Capillaroscopy in Fabry disease: Study of a family

Author(s): Lopez-Rodriguez Monica | Barbado-Hernandez Francisco | Eslava Antonio | Garcia-Consuegra Julia | Arias-Martinez Natividad | Gomez-Cerezo Jorge | Pagan-Munoz Barbara | Vazquez-Rodriguez Juan
Volume: 12
Issue: 1
Year: 2006
Prevalence of congenital heart diseases in Mysore

Author(s): Smitha R | Karat S | Narayanappa D | Krishnamurthy B | Prasanth S | Ramachandra N
Volume: 12
Issue: 1
Year: 2006
Detection of Helicobactor pylori by polymerase chain reaction: A comparison in sample preparation

Author(s): Murugesan R | Bhattacharjee P | Vivek Kumar P | Mohankumar Mary | Nagarajan Mangala | Jeevanram R
Volume: 11
Issue: 1
Year: 2005
Heterozygosity and allele frequencies of the two VNTRs (ApoB and D1S80) in Iranian population

Author(s): Mahdieh Nejat | Tafsiri Elham | Karimipour Morteza | Akbari Mohammad
Volume: 11
Issue: 1
Year: 2005
Association of erythrocyte acid phosphatase phenotypes with myopia

Author(s): Himabindu P | Vishnupriya S | Shravankumar K | Rao Vittal | Sunder Shyam
Volume: 11
Issue: 1
Year: 2005
Polymorphism of alpha-1-antitrypsin and association of S and Z alleles with duodenal ulcers

Author(s): Sulekha S | Mathur B | Pratibha N
Volume: 11
Issue: 1
Year: 2005
An understanding the genetic basis of congenital heart disease

Author(s): Ramegowda Smitha | Ramachandra Nallur
Volume: 11
Issue: 1
Year: 2005
Past, present and future perspectives of genetic therapy in gliomas

Author(s): Mattei Tobias | Ramina Ricardo | Tatagiba Marcos | Aguiar Paulo
Volume: 11
Issue: 1
Year: 2005
Opportunity for natural selection among three endogamous subpopulations of Andhra Pradesh

Author(s): Lakshmi N | Venkateswara Rao T | Veerraju P
Volume: 11
Issue: 1
Year: 2005
Loss of sex chromosome in acute myeloid leukemia

Author(s): Bakshi Sonal | Kakadia Purvi | Brahmbhatt Manisha | Trivedi Pina | Rawal Shwetal | Bhatt Samarth | Parikh Bharat | Patel Kirti | Shukla Shilin | Shah Pankaj
Volume: 10
Issue: 1
Year: 2004
Menstrual history in women with down syndrome - A review

Author(s): Ranganath Priya | Rajangam Sayee
Volume: 10
Issue: 1
Year: 2004
Quantitative variation of superoxide dismutase levels in leukaemias

Author(s): Poongothai A | Vishnupriya S | Ragunadharao D
Volume: 10
Issue: 1
Year: 2004
Association of alkaline phosphatase phenotypes with arthritides

Author(s): Padmini A | Ushasree B | Babu Ravi | Nallari Pratibha
Volume: 10
Issue: 1
Year: 2004
Heritability estimation of conventional cardiovascular disease risk factors in Asian Indian families: The Calcutta family study

Author(s): Ghosh Arnab | Dutta Rupak | Sarkar Angshuman
Volume: 16
Issue: 1
Year: 2010
Chromosomal abnormalities associated with mental retardation in female subjects

Author(s): Dutta Samikshan | Shaw Jyoti | Sinha Swagata | Mukhopadhyay Kanchan
Volume: 15
Issue: 1
Year: 2009
Y-haplotypes and idiopathic male infertility in an Indian population

Author(s): Singh Kiran | Raman Rajiva
Volume: 15
Issue: 1
Year: 2009
Glanzmann′s thrombasthenia and molecular mimicry

Author(s): Wiwanitkit Viroj
Volume: 16
Issue: 1
Year: 2010
Indian Journal of Human Genetics in PubMed: Cautious but confident steps

Author(s): Ghosh Kanjaksha
Volume: 16
Issue: 1
Year: 2010
Screening for beta thalassaemia

Author(s): Petrou Mary
Volume: 16
Issue: 1
Year: 2010
Ernest Beutler

Author(s): Ghosh Kanjaksha | Gorakshakar Ajit
Volume: 15
Issue: 1
Year: 2009
Weaver syndrome: A report of a rare genetic syndrome

Author(s): Bansal Nitin | Bansal Amit
Volume: 15
Issue: 1
Year: 2009
Radial aplasia with oligodactyly

Author(s): Panigrahi Inusha | Kulkarni Ketan
Volume: 14
Issue: 1
Year: 2008
Megarbane syndrome

Author(s): Caglayan Ahmet | Dundar Munis
Volume: 14
Issue: 1
Year: 2008
XIII International congress of histocompatibility and immunogenetics (2002)

Author(s): Shankarkumar U
Volume: 8
Issue: 1
Year: 2002
Fluorescence in situ hybridization analysis of balanced t (8;22) (q24.3;q12.2) in a female with recurrent spontaneous abortions

Author(s): Vundinti Babu Rao | kerketta Lily | Korgaonkar Seema | Ghosh Kanjaksha | Mohanty Dipika
Volume: 8
Issue: 1
Year: 2002
Catching up with the progress...

Author(s): Mohanty Dipika
Volume: 8
Issue: 1
Year: 2002
MTHFR gene polymorphisms analyzed in population from Kolkata, West Bengal

Author(s): Mukhopadhyay K | Dutta S | Das Bhomik
Volume: 13
Issue: 1
Year: 2007
Mutational spectrum of thalassemias in India

Author(s): Panigrahi Inusha | Marwaha R
Volume: 13
Issue: 1
Year: 2007
Gitelman′s syndrome

Author(s): Chowta Nithyananda | Chowta Mukta
Volume: 12
Issue: 1
Year: 2006
Stem cells: A new paradigm

Author(s): Kumar Sachin | Singh N
Volume: 12
Issue: 1
Year: 2006
PCR - From diagnostics to gene expression profiling

Author(s): Colah Roshan
Volume: 12
Issue: 1
Year: 2006
Cohen syndrome

Author(s): Kumar T | Scott Julius
Volume: 11
Issue: 1
Year: 2005
Time to form a consortium to study the genetic polymorphism by using standard DNA markers

Author(s): Ghosh K | Mukherjee M | Mohanty D
Volume: 11
Issue: 1
Year: 2005
Fluorescence in situ hybridization studies: Break apart or not?

Author(s): Bakshi Sonal | Brahmbhatt Manisha | Trivedi Pina | Rawal Shwetal | Kakadia Purvi | Bhatt Samarth
Volume: 10
Issue: 1
Year: 2004
Sex chromosome loss and malignancy: Does a relationship established?

Author(s): Mohanty Dipika
Volume: 10
Issue: 1
Year: 2004
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