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Humangenetik|January 1, 1975
Human karyotype polymorphism. III. Routine ank fluorescence microscopic investigation of chromosomes in normal adults and mentally retarded childrenA V Mikelsaar, M E Käosaar, S J Tüür, et al.Humangenetik|May 26, 1975
Sex chromatin and cytogenetic survey of 10417 adult males and 357 children institutionalized in Belgian institutions for mentally retarded patientsJ J Cassiman, J P Fryns, J De Roover, et al.Humangenetik|July 23, 1975
Chromatin structure in Down's syndromeK N Fedorova, V M Inshakova, D M SpitkovskyHumangenetik|September 10, 1975
Familial true hermaphrodism in three siblings: clinical, cytogenetic, histological and hormonal studiesS Armendares, F Salamanca, J M Cantú, et al.Humangenetik|January 1, 1975
Population genetics of human red cell phosphoclucomutase isozyme PGM3 (E.C.: 2.7.5.1). Gene frequencies in Southwestern GermanyS Bissbort, J Kömpf, R Bethge, et al.Humangenetik|January 1, 1975
Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studiesU Francke, C Kernahan, C BradshawHumangenetik|January 1, 1975
Probable loose linkage between the ABO locus and Waardenburg syndrome type IS Arias, M Mota, A Yánez, et al.Humangenetik|January 1, 1975
[Centronuclear myopathy with autosomal dominant inheritance(author's transl)]W Mortier, E Michaelis, J Becker, et al.Humangenetik|January 1, 1975
G-6PD "ankara". a new G-6PD variant with deficiency found in a Turkish familyA Kahn, M L North, J Messer, et al.Humangenetik|January 1, 1975
Dicentric Yp chromosome in a patient with the gonadal dysgenesis and gonadoblastomaJ Málková, K Michalová, R Chrz, et al.Pageof 23