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Human Genetics|January 1, 1980
Regional assignment of the gene locus for steroid sulfataseC R Müller, A Westerveld, B Migl, et al.Nucleic Acids Research|March 27, 2001
Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarraysF Erdogan, R Kirchner, W Mann, et al.The Journal of Biological Chemistry|September 15, 1990
Derivatives of somatic cell hybrids which carry the human gene locus for nephrogenic diabetes insipidus (NDI) express functional vasopressin renal V2-type receptorsD A Jans, B A van Oost, H H Ropers, et al.Human Genetics|January 1, 1983
On the genetic length of the short arm of the human X chromosomeH H Ropers, P Wieacker, T F Wienker, et al.Human Genetics|August 1, 1992
Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21I Bach, D Robinson, N Thomas, et al.Current Opinion in Genetics & Development|June 1, 1995
Mapping and cloning hereditary deafness genesF P Cremers, M Bitner-Glindzicz, M E Pembrey, et al.American Journal of Human Genetics|July 1, 1977
Evidence for preferential X-chromosome inactivation in a family with Fabry diseaseH H Ropers, T F Wienker, T Grimm, et al.Cytogenetics and Cell Genetics|January 1, 1986
Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie diseaseA Gal, B Wieringa, D F Smeets, et al.Annales De Genetique|January 1, 1980
Assignment of the gene coding for human catalase to the short arm of chromosome 11P Wieacker, C R Mueller, A Mayerova, et al.Human Genetics|June 9, 1978
Distribution of G6PD phenotypes in red blood cells of Southern African Negroids: evidence for somatic selectionH H Ropers, H W Hitzeroth, H Hameister, et al.Pageof 21