Academic Journals Database
Disseminating quality controlled scientific knowledge

Search Articles for "craniofacial genetics"

ADD TO MY LIST
 
Analysis of four DLX homeobox genes in autistic probands

Author(s): Hamilton Steven | Woo Jonathan | Carlson Elaine | Ghanem Nöel | Ekker Marc | Rubenstein John
A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines

Author(s): Boles Melissa | Wilkinson Bonney | Maxwell Andrea | Lai Lihua | Mills Alea | Nishijima Ichiko | Salinger Andrew | Moskowitz Ivan | Hirschi Karen | Liu Bin | Bradley Allan | Justice Monica
Fryns syndrome : a case associated with karyotype XO.

Author(s): Dawani Nader | Al Madhoob Abdul | Ali Fuad | Shabib F
Crouzon's syndrome: literature review

Author(s): Silva, Dorivaldo Lopes da | Palheta Neto, Francisco Xavier | Carneiro, Stéphanie Gonçalves | Palheta, Angélica Cristina Pezzin | Monteiro, Marcela | Cunha, Sarah Crestian | Nunes, Cláudio Tobias Acatauassú
Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients

Author(s): Masotti Cibele | Ornelas Camila | Splendore-Gordonos Alessandra | Moura Ricardo | Félix Têmis | Alonso Nivaldo | Camargo Anamaria | Passos-Bueno Maria
Essential role of the N-terminal region of TFII-I in viability and behavior

Author(s): Lucena Jaume | Pezzi Susana | Aso Ester | Valero Maria | Carreiro Candelas | Dubus Pierre | Sampaio Adriana | Segura Maria | Barthelemy Isabel | Zindel Marc | Sousa Nuno | Barbero José | Maldonado Rafael | Pérez-Jurado Luis | Campuzano Victoria
Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature

Author(s): Truong Hoa | Dudding Tracy | Blanchard Christopher | Elsea Sarah
Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment

Author(s): Gould Douglas | Jaafar Mohamad | Addison Mark | Munier Francis | Ritch Robert | MacDonald Ian | Walter Michael
An Integrin-Dependent Role of Pouch Endoderm in Hyoid Cartilage Development

Author(s): Crump Justin Gage | Swartz Mary E | Kimmel Charles B
Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification

Author(s): Furtado Larissa | Wooderchak-Donahue Whitney | Rope Alan | Yetman Angela | Lewis Tracey | Plant Parker | Bayrak-Toydemir Pinar
Novel mutations of TCOF1 gene in European patients with treacher Collins syndrome

Author(s): Conte Chiara | D'Apice Maria | Rinaldi Fabrizio | Gambardella Stefano | Sangiuolo Federica | Novelli Giuseppe
Why do you need a reservation system?      Save time & money - Smart Internet Solutions