Showing results (931-940 of 9,279) with videos related to
Sort By:
Pageof 928
American Journal of Medical Genetics. Part A|December 6, 2011
The 8th international research symposium on the Marfan syndrome and related conditionsReed E Pyeritz, Bart LoeysAmerican Journal of Medical Genetics. Part A|December 6, 2011
Report of a mother and daughter with the 12q14 microdeletion syndromeAudrey L Bibb, Jill A Rosenfeld, David D WeaverAmerican Journal of Medical Genetics. Part A|December 6, 2011
Consensus recommendations for current treatments and accelerating clinical trials for patients with neurofibromatosis type 2Jaishri O Blakeley, D Gareth Evans, John Adler, et al.American Journal of Medical Genetics. Part A|May 12, 2012
Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndromeKen Higashimoto, Kazuhiko Nakabayashi, Hitomi Yatsuki, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Ambiguous genitalia: what prenatal genetic testing is practical?Margaret P Adam, Patricia Y Fechner, Linda A Ramsdell, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Extracellular matrix and platelet function in patients with musculocontractural Ehlers-Danlos syndrome caused by mutations in the CHST14 geneRoberto Mendoza-Londono, David Chitayat, Walter H A Kahr, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Typical renal-coloboma syndrome phenotype in a patient with a submicroscopic deletion of the PAX2 geneKucinskas Laimutis, Craig Jackson, Xinjie Xu, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosomeJennifer N Sanmann, Danielle L Bishay, Lois J Starr, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type IGhada M H Abdel-Salam, Mohamed S Abdel-Hamid, Mahmoud Issa, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Familial Xp22.33-Xp22.12 deletion delineated by chromosomal microarray analysis causes proportionate short statureSung Yoon Cho, Chang-Seok Ki, Ja-Hyun Jang, et al.Pageof 928