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Journal of Medical Genetics|February 1, 1988
An autosomal dominant multiple pterygium syndromeC M McKeown, R HarrisClinical Genetics|August 1, 1995
Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndromeP J Renwick, A J Birley, C M McKeown, et al.Journal of Medical Genetics|February 9, 1999
Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predispositionY L Wallis, D G Morton, C M McKeown, et al.Clinical Genetics|January 1, 1994
Exclusion of an elastin gene (ELN) mutation as the cause of pseudoxanthoma elasticum (PXE) in one familyM C Raybould, A J Birley, C Moss, et al.Transplantation|August 1, 1988
Sinusoidal lining cell damage: the critical injury in cold preservation of liver allografts in the ratC M McKeown, V Edwards, M J Phillips, et al.Transplantation|June 1, 1988
Adenine nucleotide tissue concentrations and liver allograft viability after cold preservation and warm ischemiaP R Harvey, S Iu, C M McKeown, et al.Human Genetics|November 1, 1994
Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposisY L Wallis, F Macdonald, M Hultén, et al.Human Genetics|October 1, 1986
Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimationJ F Clayton, A F Wright, M Jay, et al.American Journal of Human Genetics|October 1, 1987
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14A F Wright, S S Bhattacharya, J F Clayton, et al.Pageof 2