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Human Heredity|January 1, 1987
Robustness of path analysis of family resemblance against deviations from multivariate normalityD C Rao, G P Vogler, I B Borecki, et al.Human Heredity|January 1, 1987
Genetic polymorphism of red cell glutamate-pyruvate transaminase in JapaneseT Toyomasu, M MukaidaHuman Heredity|January 1, 1987
Gc and C3 polymorphisms in South SardiniaR Floris-Masala, G Gruppioni, M Lunesu, et al.Human Heredity|January 1, 1987
Gc subtypes in some population groups from Israel. Comparison between world population groups and between Jews and non-Jews of the same areasS NevoHuman Heredity|January 1, 1986
Group-specific component (Gc): subtypes in the Finnish population. Description of a new allele and an apparent mother-child incompatibilityM Lukka, P Turunen, M Kataja, et al.Human Heredity|January 1, 1986
The Webb (Wb) antigen in South Wales donorsL Bloomfield, G P Rowe, C GreenHuman Heredity|March 28, 2022
The mitochondrial tRNAAsp T7561C, tRNAHis C12153T and A12172G mutations may be associated with essential hypertension in a Han Chinese pedigreeHaiying Fu, Jinming Sun, Xiaoyan XuHuman Heredity|January 1, 1986
Phosphoglycolate phosphatase polymorphism: gene frequencies in three Italian samplesC Santolamazza, A Benincasa, R ScozzariHuman Heredity|January 1, 1979
Some aspects of the occurrence of new mutations in haemophiliaR Ananthakrishnan, S D'SouzaPageof 237