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American Journal of Human Genetics|November 1, 1983
Differences in the frequency of X-linked deleterious genes in human populationsA Chakravarti, S J BaleAmerican Journal of Medical Genetics|January 1, 1990
Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant geneJ A Badner, A ChakravartiAmerican Journal of Human Genetics|September 1, 1991
Cleft lip and palate: no evidence of linkage to transforming growth factor alphaJ T Hecht, Y P Wang, S H Blanton, et al.Lancet (London, England)|February 1, 1986
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuriaS P Daiger, A S Lidsky, R Chakraborty, et al.Human Genetics|January 1, 1995
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated familyR E McGuire, A M Gannon, L S Sullivan, et al.Genomics|September 1, 1990
Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3qS H Blanton, A W Cottingham, N Giesenschlag, et al.American Journal of Medical Genetics|August 1, 1992
Clinical variability and genetic heterogeneity within the Acadian Usher populationR J Smith, M Z Pelias, S P Daiger, et al.Biochemical and Biophysical Research Communications|November 27, 1985
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2L Chan, P VanTuinen, D H Ledbetter, et al.Genomics|October 1, 1989
Multilocus linkage analysis with the human argininosuccinate synthetase geneH Northrup, M Lathrop, S Y Lu, et al.International Journal of Pediatric Otorhinolaryngology|March 27, 2013
Cutaneous mucormycosis of nose and facial region in children: a case seriesA Chakravarti, R Bhargava, S BhattacharyaPageof 27