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Genomics|March 1, 1991
A genetic linkage map of 27 markers on human chromosome 21M B Petersen, S A Slaugenhaupt, J G Lewis, et al.Proceedings of the National Academy of Sciences of the United States of America|September 12, 1995
Molecular characterization of a second melatonin receptor expressed in human retina and brain: the Mel1b melatonin receptorS M Reppert, C Godson, C D Mahle, et al.American Journal of Medical Genetics|November 20, 1995
Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33C M Eng, S A Slaugenhaupt, A Blumenfeld, et al.Genomics|May 20, 1995
Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a)S A Slaugenhaupt, A L Roca, C B Liebert, et al.Human Genetics|August 1, 1991
Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeatM B Petersen, J L Weber, S A Slaugenhaupt, et al.American Journal of Human Genetics|August 12, 1999
Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypesS A Slaugenhaupt, J S Acierno, L A Helbling, et al.American Journal of Human Genetics|April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17P I Patel, B Franco, C Garcia, et al.Science (New York, N.Y.)|August 7, 1987
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndromeA C Warren, A Chakravarti, C Wong, et al.American Journal of Human Genetics|January 1, 1989
Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markersS D Kittur, M M Bagdon, M L Lubs, et al.Annals of Human Genetics|March 30, 2000
Report and abstracts of the Sixth International Workshop on chromosome 9B P Chadwick, L J Campbell, C L Jackson, et al.Pageof 4