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P R Fain

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Human Heredity|May 1, 1995

Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1M A Pericak-Vance, D F Barker, J A Bergoffen, et al.

Human Genetics|December 1, 1991

High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markersD F Barker, P R Fain, D E Goldgar, et al.

Genes and Immunity|August 25, 2006

Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac diseaseJ R Bilbao, B Calvo, A M Aransay, et al.

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Search research articles

Showing results (51-60 of 53) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 53 results.

Human Heredity|May 1, 1995

Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1M A Pericak-Vance, D F Barker, J A Bergoffen, et al.

Human Genetics|December 1, 1991

High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markersD F Barker, P R Fain, D E Goldgar, et al.

Genes and Immunity|August 25, 2006

Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac diseaseJ R Bilbao, B Calvo, A M Aransay, et al.

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