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Genome Research|April 1, 1996
Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contigR E McGuire, S A Jordan, V V Braden, et al.American Journal of Medical Genetics|March 15, 1996
Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11S H Blanton, D Hogue, M Wagner, et al.Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|November 1, 1996
Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosisN H Miller, B Mims, A Child, et al.Genetic Testing|January 1, 1997
Implications of molecular diagnostic testing in families with hereditary pancreatitisA Pandya, X J Xia, S H Blanton, et al.American Journal of Human Genetics|July 1, 1985
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuriaA S Lidsky, F D Ledley, A G DiLella, et al.American Journal of Human Genetics|May 1, 1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, et al.Genomics|December 1, 1996
Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7qA Pandya, S H Blanton, B Landa, et al.American Journal of Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU)S P Daiger, R Chakraborty, L Reed, et al.Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.American Journal of Human Genetics|March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasiaM Deere, S H Blanton, C I Scott, et al.Pageof 12