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Clinical Genetics|November 1, 1994
Familial translocation (X;3) (p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern studyD Bettio, N Rizzi, D GiardinoClinical Genetics|November 1, 1994
Identification of a non-fluorescent isodicentric Y chromosome by molecular cytogenetic techniquesM J Macera, J Sherman, H O Shah, et al.Clinical Genetics|November 1, 1994
Patient with de novo 12p+ syndrome identified as dir dup (12) (p13) using subchromosomal painting libraries from somatic cell hybridsL Zelante, S Calvano, B Dallapiccola, et al.Clinical Genetics|November 1, 1994
Antley-Bixler syndrome: report of a patient and review of literatureS Hassell, M G ButlerClinical Genetics|December 1, 1994
Association between genetic variation at the APO AI-CIII-AIV gene cluster and familial combined hyperlipidaemiaC F Xu, P Talmud, H Schuster, et al.Clinical Genetics|December 1, 1994
Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like featuresG Oğur, N Baykan, A De Paepe, et al.Clinical Genetics|December 1, 1994
Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplicationU Moog, J J Engelen, C E de Die-Smulders, et al.Clinical Genetics|December 1, 1994
Single mandibular incisor in a patient with del (18p) anomalyR A Pfeiffer, K Hertrich, M CohenClinical Genetics|December 1, 1994
No effect on blood pressure level or variability of polymorphisms in DNA at the locus for atrial natriuretic factor (ANF)K E Berge, K BergClinical Genetics|December 1, 1994
No effect of a BglI polymorphism at the renin (REN) locus on blood pressure level or variabilityK E Berge, K BergPageof 718