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American Journal of Medical Genetics|October 23, 1995
Opitz GBBB syndrome: chromosomal evidence of an X-linked formA Verloes, A David, S Odent, et al.American Journal of Medical Genetics|October 23, 1995
Prenatal diagnosis of a stable de novo centric fission: a case reportM H Bogart, N Fujita, L Serles, et al.American Journal of Medical Genetics|October 23, 1995
Interstitial deletion of the long arm of chromosome 6 associated with unusual limb anomalies: report of two new patients and review of the literatureA Pandya, N Braverman, R E Pyeritz, et al.American Journal of Medical Genetics|October 23, 1995
Hypoglycemia in Coffin-Siris syndromeK Imaizumi, M Nakamura, M Masuno, et al.American Journal of Medical Genetics|October 23, 1995
Barriers to carrier testing for adult cystic fibrosis sibs: the importance of not knowingJ H Fanos, J P JohnsonAmerican Journal of Medical Genetics|October 23, 1995
Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome?K H Orstavik, P Strömme, S Spetalen, et al.American Journal of Medical Genetics|July 26, 1996
Ernst Rüdin (1874-1952) and his genealogic-demographic department in Munich (1917-1986): an introduction to their family studies of schizophreniaE Zerbin-Rüdin, K S KendlerAmerican Journal of Medical Genetics|July 26, 1996
New phenotype definition of attention deficit hyperactivity disorder in relatives for genetic analysesS Milberger, S V Faraone, J Biederman, et al.American Journal of Medical Genetics|July 26, 1996
Family patterns of developmental dyslexia. Part III: Spelling errors as behavioral phenotypeP H Wolff, I Melngailis, K KotwicaAmerican Journal of Medical Genetics|July 26, 1996
Characterization of six mutations in exon 37 of neurofibromatosis type 1 geneM Upadhyaya, M Osborn, J Maynard, et al.Pageof 854