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F J Smith

Showing results (111-120 of 117) with videos related to

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Health Management Technology|June 6, 1997
Enterprise integration. The CIO tapes. Roundtable discussionM Anderson, L Bates, R D Brickman, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Cell|January 10, 1997
Targeted disruption of the melanocortin-4 receptor results in obesity in miceD Huszar, C A Lynch, V Fairchild-Huntress, et al.
The British Journal of Dermatology|February 21, 1998
Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated casesJ E Mellerio, F J Smith, J R McMillan, et al.
American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.
Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, 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.
Pageof 12

Showing results (111-120 of 117) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 117 results.
Health Management Technology|June 6, 1997
Enterprise integration. The CIO tapes. Roundtable discussionM Anderson, L Bates, R D Brickman, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Cell|January 10, 1997
Targeted disruption of the melanocortin-4 receptor results in obesity in miceD Huszar, C A Lynch, V Fairchild-Huntress, et al.
The British Journal of Dermatology|February 21, 1998
Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated casesJ E Mellerio, F J Smith, J R McMillan, et al.
American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.
Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, 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.
Pageof 12