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A R. Curtis

Showing results (11-20 of 16) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1994
A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28A R Curtis, S Lindsay, E Boye, et al.
Gene|April 11, 1997
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25T D Bui, M Lako, S Lejeune, et al.
Genomics|July 1, 1993
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosomeS Lindsay, A R Curtis, P Roustan, 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.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
European Journal of Human Genetics : EJHG|January 1, 1994
A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28A R Curtis, S Lindsay, E Boye, et al.
Gene|April 11, 1997
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25T D Bui, M Lako, S Lejeune, et al.
Genomics|July 1, 1993
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosomeS Lindsay, A R Curtis, P Roustan, 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.
Pageof 2