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Human Genetics|October 2, 1979
A low frequency mosaicism for monosomy 21 in a live born femaleM Lee, D Rose, A Lazzarini, et al.Human Genetics|November 1, 1979
De novo 13q paracentric inversion in a boy with cleft palate and mental retardationV M Riccardi, G P HolmquistHuman Genetics|April 5, 1979
Two cases of familial paracentric inversion in man associated with sex chromosome anomaly. 47,XXY,inv(5)(q21q32) and 45,X,inv(7)(q11.3q22.3)N Canki, B DutrillauxHuman Genetics|April 5, 1979
Characterisation of the isoenzymes of phosphoglucomutase (PGM) determined by the first (PGM1) and second (PGM2) locus observed by isoelectric focusingJ G SuttonHuman Genetics|April 5, 1979
Electrophoretic demonstration of heterozygosis in hereditary pyruvate kinase deficiency. An unusual methodA Kahn, J Marie, J L Vives-CorronsHuman Genetics|April 17, 1979
Los Angeles variant of galactose-1-phosphate uridyltransferase (EC 2.7.7.12) in a Mexican familyB Ibarra, G Vaca, J Sánchez-Corona, et al.Human Genetics|April 17, 1979
Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21)J P Fryns, N Logghe, M Van Eygen, et al.Human Genetics|April 17, 1979
Relationship between alpha-L-fucosidase deficiency in plasma and alpha-L-fucosidase activity in leukocytesR Gatti, S Cavalieri, G RomeoHuman Genetics|April 17, 1979
Sister chromatid exchange and cell cycle in fibroblasts of Bloom's syndromeS V BratHuman Genetics|April 27, 1979
The occurrence of DChi and new D and B transferrin variants among caste groups of Andhra Pradesh (S. India)P R Rao, J D Goud, B R SwamyPageof 957