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S A Jordan

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Human Mutation|January 1, 1993

A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplexM M Humphries, D M Sheils, G J Farrar, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999

A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23E H Simpson, R Suffolk, J A Bell, et al.

Nature Genetics|May 1, 1993

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qS A Jordan, G J Farrar, P Kenna, et al.

Human Mutation|January 1, 1996

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of IrelandM M Humphries, F C Mansergh, A S Kiang, et al.

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Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 44 results.

Human Mutation|January 1, 1993

A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplexM M Humphries, D M Sheils, G J Farrar, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999

A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23E H Simpson, R Suffolk, J A Bell, et al.

Nature Genetics|May 1, 1993

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qS A Jordan, G J Farrar, P Kenna, et al.

Human Mutation|January 1, 1996

Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of IrelandM M Humphries, F C Mansergh, A S Kiang, et al.

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