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American Journal of Medical Genetics|December 18, 2001
High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22)A M Francisco-Bagnariolli, S L Payão, R S Kawasaki-Oyama, et al.American Journal of Medical Genetics|December 18, 2001
Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutationS Abe, P M Kelley, W J Kimberling, et al.American Journal of Medical Genetics|December 18, 2001
Secular trends in congenital anomaly-related fetal and infant mortality in Canada, 1985-1996S Liu, K S Joseph, S W Wen, et al.American Journal of Medical Genetics|December 18, 2001
Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysisM A Rigola, A Plaja, C Mediano, et al.American Journal of Medical Genetics|December 18, 2001
Persistence of Müllerian derivatives and intestinal lymphangiectasis in two newborn brothers: confirmation of the Urioste syndromeC Bellini, E Bonioli, N Josso, et al.American Journal of Medical Genetics|December 18, 2001
Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndromeC L Barr, L Best, R WeksbergAmerican Journal of Medical Genetics|December 18, 2001
Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian familyM Ghadami, K Majidzadeh-A, B S Haerian, et al.American Journal of Medical Genetics|December 18, 2001
Clinical value of postnatal autopsy and genetics consultation in fetal deathL A Hefler, D R Hersh, P J Moore, et al.American Journal of Medical Genetics|December 26, 2001
Acampomelic campomelic syndromeU Moog, N J Jansen, G Scherer, et al.American Journal of Medical Genetics|December 26, 2001
Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrencesK L Russell, J E Ming, K Patel, et al.Pageof 854