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S P Bryant

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Human Molecular Genetics|May 20, 1999

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.

Nature Genetics|August 1, 1996

Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.

Annals of Human Genetics|November 1, 1996

European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme HumainS A Cox, J Attwood, S P Bryant, et al.

Nature|May 20, 2006

The DNA sequence and biological annotation of human chromosome 1S G Gregory, K F Barlow, K E McLay, et al.

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Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

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

Human Molecular Genetics|May 20, 1999

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.

Nature Genetics|August 1, 1996

Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.

Annals of Human Genetics|November 1, 1996

European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme HumainS A Cox, J Attwood, S P Bryant, et al.

Nature|May 20, 2006

The DNA sequence and biological annotation of human chromosome 1S G Gregory, K F Barlow, K E McLay, et al.

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