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Human Heredity|January 1, 1991
Phosphoglucomutase-1 subtypes in two populations in Adriatic islands: presence of PGM1*W3 (PGM1*7+) alleleN Borot, J Arnaud, P Rudan, et al.Human Heredity|January 1, 1991
C1R subcomponent polymorphism in Japanese: description of a new alleleA Kido, N Komatsu, Y Kimura, et al.Human Heredity|January 1, 1991
Plasminogen polymorphism in Libyans: description of a new rare variantI M SebetanHuman Heredity|January 1, 1991
Acid phosphatase, adenosine deaminase and esterase D polymorphisms in the Spanish Basque populationA I Aguirre, A Vicario, L I Mazón, et al.Human Heredity|April 3, 2025
A Bibliometric Analysis of GWAS on Rheumatoid Arthritis from 2002 to 2024Wen-Hui Wang, Ming-Hui Xia, Xin-Ru Liu, et al.Human Heredity|March 17, 1999
Human NDUFB9 gene: genomic organization and a possible candidate gene associated with deafness disorder mapped to chromosome 8q13X Lin, D E Wells, W J Kimberling, et al.Human Heredity|March 17, 1999
No correlation between A(-1438)G polymorphism in 5-HT2A receptor gene promoter and the density of frontal cortical 5-HT2A receptors in schizophreniaA P Kouzmenko, A Scaffidi, A M Pereira, et al.Human Heredity|January 1, 1990
Transferrin subtypes and spontaneous abortion in a Chinese populationN Saha, J S Tay, B Murugasu, et al.Human Heredity|April 11, 2013
A rapid association test procedure robust under different genetic models accounting for population stratificationWenan Chen, Xiangning Chen, Kellie J Archer, et al.Human Heredity|January 1, 1990
Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndromeE J Devor, D K Grandy, O Civelli, et al.Pageof 237