Showing results (1231-1240 of 9,284) with videos related to
Sort By:
Pageof 929
American Journal of Medical Genetics. Part A|November 26, 2009
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European originElisabeth Mangold, Heiko Reutter, Stefanie Birnbaum, et al.American Journal of Medical Genetics. Part A|November 26, 2009
"It's something I need to consider": decisions about carrier screening for fragile X syndrome in a population of non-pregnant womenAlison D Archibald, Alice M Jaques, Samantha Wake, et al.American Journal of Medical Genetics. Part A|November 26, 2009
Pseudoaminopterin syndrome: clinical report with new characteristicsN Sobreira, M Cernach, D Batista, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Paternal balanced reciprocal translocation t(9;22)(q34.3;q11.2) resulting in an infant with features of the 9q subtelomere and the 22q11 deletion syndromes due to 3:1 meiotic segregation and tertiary monosomyRobin R McGoey, Yves LacassieAmerican Journal of Medical Genetics. Part A|October 31, 2009
Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pterCarlos A Tirado, Samuel Henderson, Naseem Uddin, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirthGordana Raca, Amber Artzer, Laura Thorson, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Premolar hypodontia is a common feature in Sotos syndrome with a mutation in the NSD1 geneJohanna Kotilainen, Pia Pohjola, Sinikka Pirinen, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Psychosocial aspects of patients with Niemann-Pick disease, type BShelly L Henderson, Wendy Packman, Seymour PackmanAmerican Journal of Medical Genetics. Part A|November 10, 2005
A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu syndromeTiong Yang Tan, Agnes Bankier, Howard R Slater, et al.American Journal of Medical Genetics. Part A|September 27, 2014
Duodenal atresia in 17q12 microdeletion including HNF1B: a new associated malformation in this syndromeFabiola Quintero-Rivera, Jennifer S Woo, Eric M Bomberg, et al.Pageof 929