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Human Genetics|August 1, 1993
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palateC Stoll, J F Qian, J Feingold, et al.Human Genetics|September 1, 1993
Two new polymorphisms in introns 2 and 3 of the human porphobilinogen deaminase geneM Daimon, Y Morita, K Yamatani, et al.Human Genetics|September 1, 1993
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.Human Genetics|October 1, 1993
Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locusA Nordenskjöld, F Hedborg, H Luthman, et al.Human Genetics|March 1, 1994
The spatial localization of homologous chromosomes in human fibroblasts at mitosisA R Leitch, J K Brown, W Mosgöller, et al.Human Genetics|March 1, 1994
Mutation screening by a combination of biotin-SSCP and direct sequencingA S Virdi, J A Loughlin, C M Irven, et al.Human Genetics|March 1, 1994
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2)P S Rowe, J Goulding, A Read, et al.Human Genetics|March 1, 1994
Linkage mapping of the spinal muscular atrophy geneA H Burghes, S E Ingraham, Z Kóte-Jarai, et al.Human Genetics|March 1, 1994
Prevalence of beta allele of the insulin gene in type II diabetes mellitusW Horst-Sikorska, B Zoll, J Kwiatkowska, et al.Human Genetics|March 1, 1994
Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.Pageof 957