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American Journal of Medical Genetics. Part A|August 5, 2011
Automated syndrome detection in a set of clinical facial photographsStefan Boehringer, Manuel Guenther, Stella Sinigerova, et al.American Journal of Medical Genetics. Part A|August 5, 2011
Limb-body wall defect. Is there a defensible hypothesis and can it explain all the associated anomalies?Alasdair G W Hunter, Laurie H Seaver, Roger E StevensonAmerican Journal of Medical Genetics. Part A|August 12, 2011
Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritancePelin Özlem Şimşek Kiper, Gülen Eda Utine, Koray Boduroğlu, et al.American Journal of Medical Genetics. Part A|August 12, 2011
Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay populationIman Salahshourifar, Wan Azman Wan Sulaiman, Bin Alwi Zilfalil, et al.American Journal of Medical Genetics. Part A|August 12, 2011
Variants in genes that encode muscle contractile proteins influence risk for isolated clubfootKatelyn S Weymouth, Susan H Blanton, Michael J Bamshad, et al.American Journal of Medical Genetics. Part A|August 12, 2011
Noncompaction of the left ventricular myocardium in a boy with a novel chromosome 8p23.1 deletionJoshua J Blinder, Hugo R Martinez, William J Craigen, et al.American Journal of Medical Genetics. Part A|August 12, 2011
Features of basal cell carcinomas in basal cell nevus syndromeWynnis L Tom, M Yadira Hurley, Dana S Oliver, et al.American Journal of Medical Genetics. Part A|July 9, 2011
A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian familyMasoud Garshasbi, Kimia Kahrizi, Masoumeh Hosseini, et al.American Journal of Medical Genetics. Part A|July 9, 2011
Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrumDenise Horn, Peter Krawitz, Anca Mannhardt, et al.American Journal of Medical Genetics. Part A|July 9, 2011
Discovery of genetic susceptibility factors for human birth defects: an opportunity for a National AgendaAndrew F Olshan, Charlotte A Hobbs, Gary M ShawPageof 928