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American Journal of Medical Genetics. Part A|September 10, 2005
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing lossHuijun Yuan, Yaping Qian, Yanjun Xu, et al.American Journal of Medical Genetics. Part A|September 10, 2005
Autosomal recessive Oliver-McFarlane syndrome: retinitis pigmentosa, short stature (GH deficiency), trichomegaly, and hair anomalies or CPD syndrome (chorioretinopathy-pituitary dysfunction)Motti Haimi, Ruth Gershoni-BaruchAmerican Journal of Medical Genetics. Part A|August 6, 2005
A patient with mosaic partial trisomy 18 resulting from dicentric chromosome breakageJennifer J D Morrissette, Livija Medne, Tyrone Bentley, et al.American Journal of Medical Genetics. Part A|August 6, 2005
Geneticists' views on science policy formation and public outreachDebra J H Mathews, Andrea Kalfoglou, Kathy HudsonAmerican Journal of Medical Genetics. Part A|September 8, 2005
SOX2 mutation causes anophthalmia, hearing loss, and brain anomaliesStephanie A Hagstrom, Gayle J T Pauer, Janet Reid, et al.American Journal of Medical Genetics. Part A|September 15, 2005
Ring chromosome 9 [r(9)(p24q34)]: a report of two casesSmita M Purandare, Jiyun Lee, Susan Hassed, et al.American Journal of Medical Genetics. Part A|September 15, 2005
Precision and error of three-dimensional phenotypic measures acquired from 3dMD photogrammetric imagesKristina Aldridge, Simeon A Boyadjiev, George T Capone, et al.American Journal of Medical Genetics. Part A|September 15, 2005
Facial and physical features of Aicardi syndrome: infants to teenagersV Reid Sutton, Bobbi J Hopkins, Tanya N Eble, et al.American Journal of Medical Genetics. Part A|September 15, 2005
Prenatal magnetic resonance imaging in Gomez-Lopez-Hernandez syndrome and review of the literatureTiong Yang Tan, George McGillivray, Stacy K Goergen, et al.American Journal of Medical Genetics. Part A|September 10, 2005
Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effectValérie Delague, Eliane Chouery, Sandra Corbani, et al.Pageof 928