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American Journal of Medical Genetics. Part A|November 24, 2004
A novel syndrome resembling Desbuquois dysplasiaAli Al Kaissi, N Nessib, M B Ghachem, et al.American Journal of Medical Genetics. Part A|December 8, 2004
Supernumerary ring chromosome 7 mosaicism: case report, investigation of the gene content, and delineation of the phenotypeK D Lichtenbelt, R Hochstenbach, W M van Dam, et al.American Journal of Medical Genetics. Part A|June 7, 2005
Application of a comprehensive protocol for the identification of Gaucher disease in BrazilKristiane Michelin, Alessandro Wajner, Fernanda T S de Souza, et al.American Journal of Medical Genetics. Part A|June 9, 2005
Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterizationMattia Gentile, Paolo Volpe, Filomena Cariola, et al.American Journal of Medical Genetics. Part A|June 9, 2005
PTPN11 mutations play a minor role in isolated congenital heart diseaseConstance G Weismann, A Hager, H Kaemmerer, et al.American Journal of Medical Genetics. Part A|June 9, 2005
Generalized arterial calcification of infancy: different clinical courses in two affected siblingsKun-Shan Cheng, Ming-Ren Chen, Nico Ruf, et al.American Journal of Medical Genetics. Part A|June 9, 2005
Terminal deletion of 6p results in a recognizable phenotypeRuth J Lin, Athena M Cherry, Kelly C Chen, et al.American Journal of Medical Genetics. Part A|June 7, 2005
Cause of sudden, unexpected death of Prader-Willi syndrome patients with or without growth hormone treatmentT Nagai, K Obata, H Tonoki, et al.American Journal of Medical Genetics. Part A|June 7, 2005
Reported multivitamin consumption and the occurrence of multiple congenital anomaliesNataliya Yuskiv, Margaret A Honein, Cynthia A MooreAmerican Journal of Medical Genetics. Part A|June 7, 2005
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pterH L Archer, S Gupta, S Enoch, et al.Pageof 928