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American Journal of Medical Genetics. Part A|February 26, 2005
Place of preimplantation diagnosis in genetic practiceAnver Kuliev, Yury Verlinsky
American Journal of Medical Genetics. Part A|March 1, 2005
Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutationPhilippe Debeer, Christel Huysmans, Wim J M Van de Ven, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomesNatalia V Kovaleva, David E Mutton
American Journal of Medical Genetics. Part A|February 4, 2005
Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopiaChang Y Tsao, Gail D Wenger, Dennis W Bartholomew
American Journal of Medical Genetics. Part A|February 4, 2005
Chromosome 18 aberrations and epilepsy: a reviewS Grosso, L Pucci, R M Di Bartolo, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith-Magenis syndrome should contain the RAI1 geneChristopher N Vlangos, Meredith Wilson, Jan Blancato, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Natural history of cardiac involvement in geleophysic dysplasiaA Scott, S Yeung, D F Dickinson, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Frequency of incidental intracranial aneurysms in neurofibromatosis type 1Wouter I Schievink, Mary Riedinger, M Marcel Maya
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