Showing results (51-60 of 204) with videos related to
Sort By:
Pageof 21
Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.Annals of Human Genetics|January 1, 1987
Localization of MIC5 to the region between HPRT and G6PD on the human X chromosomeR Hope, S Goss, E Solomon, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 11, 2000
Classical and molecular cytogenetics of the pufferfish Tetraodon nigroviridisF Grützner, G Lütjens, C Rovira, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1980
[Propionic acidemia associated with hypertrophic pyloric stenosis and bouts of severe hyperglycemia (author's transl)]W Lehnert, A Junker, H Wehinger, et al.Human Genetics|January 1, 1981
Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrationsH H Ropers, B Migl, J Zimmer, et al.Human Genetics|January 1, 1985
X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal XqA Gal, J Mücke, H Theile, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 14, 2000
Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridisB Brunner, F Grützner, M L Yaspo, et al.Human Genetics|January 25, 1979
Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfataseH Hameister, G Wolff, C H Lauritzen, et al.Genomics|July 15, 1996
The MAS proto-oncogene is not imprinted in humansA M Riesewijk, M T Schepens, E M Mariman, et al.Science (New York, N.Y.)|October 22, 1993
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase AH G Brunner, M Nelen, X O Breakefield, et al.Pageof 21