Showing results (1221-1230 of 9,283) with videos related to
Sort By:
Pageof 929
American Journal of Medical Genetics. Part A|December 17, 2009
Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and backKatherine A Rauen, Lisa Schoyer, Frank McCormick, et al.American Journal of Medical Genetics. Part A|December 17, 2009
Morphometric analysis and classification of the facial phenotype associated with fetal alcohol syndrome in 5- and 12-year-old childrenTinashe E M Mutsvangwa, Ernesta M Meintjes, Dennis L Viljoen, et al.American Journal of Medical Genetics. Part A|December 25, 2009
An unusual severe vascular case of pseudoxanthoma elasticum presenting as generalized arterial calcification of infancyG Le Boulanger, C Labrèze, A Croué, et al.American Journal of Medical Genetics. Part A|December 25, 2009
Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndromeLaila Rifai, Marylin Port-Lis, Anne-Claude Tabet, et al.American Journal of Medical Genetics. Part A|December 25, 2009
Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: identification of a 7.2-kb microdeletion using oligonucleotide tiling microarraySatoshi Narumi, Chikahiko Numakura, Takashi Shiihara, et al.American Journal of Medical Genetics. Part A|December 8, 2005
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosomeLeslie D Kulikowski, Laurie A Christ, Sintia I Nogueira, et al.American Journal of Medical Genetics. Part A|December 8, 2005
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMCThomas Liehr, Heike Starke, Gabriele Senger, et al.American Journal of Medical Genetics. Part A|December 8, 2005
Adverse reproductive outcomes among pregnancies of aunts and (spouses of) uncles in Irish families with neural tube defectsJulianne Byrne, Susan CarolanAmerican Journal of Medical Genetics. Part A|December 8, 2005
Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiencyMohammed Tredano, David N Cooper, Manfred Stuhrmann, et al.American Journal of Medical Genetics. Part A|November 19, 2009
Nonsyndromic alar clefts: report of five Brazilian patientsAntonio Richieri-Costa, Maria Leine Guion-AlmeidaPageof 929