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Clinical Genetics|February 16, 2002
Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndromeT Takahashi, I Takahashi, M Komatsu, et al.Clinical Genetics|February 16, 2002
Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patientsI Bariş, M O Kilinç, A TolunClinical Genetics|August 1, 1996
Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the motherC Apacik, M Cohen, M Jakobeit, et al.Clinical Genetics|August 1, 1996
Poland sequence in two siblings suggesting an autosomal inheritance transmissionA Cohen, S Zecca, A Dassori, et al.Clinical Genetics|June 1, 1977
Penetrance and expressivity of the gene responsible for the Gardner syndromeE W Naylor, E J GardnerClinical Genetics|June 1, 1977
Somatic segregation and Fanconi anemiaR Berger, A Bussel, C SchenmetzlerClinical Genetics|June 1, 1977
Aglossia-adactylia syndrome (special emphasis on the inheritance pattern)E Tuncbilek, C Yalcin, M AtasuClinical Genetics|August 1, 1977
Bloom's syndrome in two Dutch familiesT W Hustinx, B G Ter Haar, J M Scheres, et al.Clinical Genetics|May 3, 2006
High prevalence of the IVS 1 + 1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2P Seeman, I SakmaryováClinical Genetics|December 1, 1976
Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11)W Fu, D S Borgaonkar, P P Ladewig, et al.Pageof 718