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Human Genetics|January 1, 1983
Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosomeP Wieacker, K E Davies, B Mevorah, et al.Biochemical and Biophysical Research Communications|June 30, 2000
Isolation of two novel human RhoGEFs, ARHGEF3 and ARHGEF4, in 3p13-21 and 2q22S Thiesen, S Kübart, H H Ropers, et al.Cytogenetics and Cell Genetics|January 1, 1983
An XX male with a single STS gene doseP Wieacker, J Voiculescu, C R Müller, et al.Human Genetics|February 11, 1977
Tentative evidence for 3--4 haematopoetic stem cells in manH W Hitzeroth, K Bender, H H Ropers, et al.European Journal of Pediatrics|October 1, 1983
Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literatureM Münke, K Kruse, M Goos, et al.Human Genetics|October 1, 1989
Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophyH J Smeets, H G Brunner, H H Ropers, et al.Human Genetics|October 1, 1986
Regional localisation of X chromosome short arm probesK Paulsen, S Forrest, G Scherer, et al.Genomics|March 2, 1999
Comparative mapping of mouse and rat chromosomes by fluorescence in situ hybridizationF Grützner, H Himmelbauer, M Paulsen, et al.Human Genetics|September 1, 1988
Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotidesB Smeets, J Poddighe, H Brunner, et al.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.Pageof 21