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A R Curtis

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Human Molecular Genetics|May 1, 1993

Dinucleotide repeat polymorphism at the DXS556 locusD L Thiselton, S Kamakari, A R Curtis, et al.

Human Genetics|January 1, 1993

X chromosome linkage studies in familial Rett syndromeA R Curtis, S Headland, S Lindsay, et al.

Nature Genetics|July 5, 2001

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.

Nature Genetics|January 1, 1997

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyQ Y Li, R A Newbury-Ecob, J A Terrett, et al.

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Search research articles

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Sort By:

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You have reached the last page of results.This site can display upto 24 results.

Human Molecular Genetics|May 1, 1993

Dinucleotide repeat polymorphism at the DXS556 locusD L Thiselton, S Kamakari, A R Curtis, et al.

Human Genetics|January 1, 1993

X chromosome linkage studies in familial Rett syndromeA R Curtis, S Headland, S Lindsay, et al.

Nature Genetics|July 5, 2001

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.

Nature Genetics|January 1, 1997

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyQ Y Li, R A Newbury-Ecob, J A Terrett, et al.

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