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Human Genetics|January 1, 1994
Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumoursP A Crossey, K Foster, F M Richards, et al.Human Genetics|January 1, 1994
Isolation and characterization of the human genomic locus coding for the putative metastasis control gene nm23-H1S Dooley, T Seib, M Engel, et al.Human Genetics|January 1, 1994
Population screening of lactate dehydrogenase deficiencies in Fukuoka Prefecture in Japan and molecular characterization of three independent mutations in the lactate dehydrogenase-B(H) geneM Maekawa, K Sudo, K Nagura, et al.Human Genetics|May 22, 2017
Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization studySara Lindström, Marine Germain, Marta Crous-Bou, et al.Human Genetics|January 1, 1986
Confirmation of the close linkage between the loci for human apolipoproteins AI and AIV by the use of a cloned cDNA probe and two restriction site polymorphismsS Rogne, O Myklebost, B Olaisen, et al.Human Genetics|January 1, 1986
Restriction fragment length polymorphisms in the D7S1 region of human chromosome 7B CarrittHuman Genetics|February 1, 1986
Assignment of the human tissue-type plasminogen activator gene (PLAT) to chromosome 8J H Verheijen, R Visse, J T Wijnen, et al.Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.Human Genetics|January 1, 1985
Localization of genes encoding apolipoproteins CI, CII, and E to the p13----cen region of human chromosome 19J Scott, T J Knott, D J Shaw, et al.Human Genetics|January 1, 1985
Telomeric association in a malignant fibrous histiocytomaN Mandahl, S Heim, U Kristoffersson, et al.Pageof 958