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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 22, 2001
Folding defects in fibrillar collagensP H ByersHuman Molecular Genetics|April 18, 1998
Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the menkes protein and produces the occipital horn syndromeM Qi, P H ByersNature|July 25, 1985
Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type IIJ Bonadio, P H ByersAnnual Review of Medicine|January 1, 1994
Molecular basis of hereditary disorders of connective tissueD J Tilstra, P H ByersAnnals of the New York Academy of Sciences|January 1, 1985
Molecular basis of clinical heterogeneity in the Ehlers-Danlos syndromeP H Byers, K A HolbrookAmerican Journal of Medical Genetics|September 1, 1989
Skin is a window on heritable disorders of connective tissueK A Holbrook, P H ByersProceedings of the National Academy of Sciences of the United States of America|August 1, 1981
Reduced secretion of structurally abnormal type I procollagen in a form of osteogenesis imperfectaG S Barsh, P H ByersThe Journal of Biological Chemistry|April 15, 1992
Defective folding and stable association with protein disulfide isomerase/prolyl hydroxylase of type I procollagen with a deletion in the pro alpha 2(I) chain that preserves the Gly-X-Y repeat patternS D Chessler, P H ByersPageof 39