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Human Genetics|March 1, 1987
Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19qU Friedrich, H Brunner, D Smeets, et al.Human Genetics|April 1, 1987
Further evidence for genetic heterogeneity in the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.Human Genetics|August 12, 2017
MtDNA genomes reveal a relaxation of selective constraints in low-BMI individuals in a Uyghur populationHong-Xiang Zheng, Lei Li, Xiao-Yan Jiang, et al.Human Genetics|October 1, 1986
A 45,X male with a Yp/18 translocationE Maserati, F Waibel, B Weber, et al.Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.Human Genetics|November 1, 1986
Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12S Kølvraa, T A Kruse, P K Jensen, et al.Human Genetics|November 1, 1986
Chromosome assignment and restriction fragment length polymorphism analysis of the anonymous DNA probe B79a at 7q22 (HMG8 assignment D7S13)X Estivill, J Schmidtke, R Williamson, et al.Human Genetics|September 1, 1986
Attenuated activities and structural alterations of arylsulfatase A in tissues from subjects with pseudo arylsulfatase A deficiencyH Kihara, W E Meek, A L FluhartyHuman Genetics|December 1, 1986
Localisation of the gene for Hunter syndrome on the long arm of X chromosomeM Upadhyaya, M Sarfarazi, J S Bamforth, et al.Human Genetics|December 1, 1986
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid libraryL Bufton, T K Mohandas, R E Magenis, et al.Pageof 958