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J G Compton

Showing results (31-40 of 44) with videos related to

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The Journal of Investigative Dermatology|February 11, 1998
A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral alleleT N Darling, B B Koh, S J Bale, et al.
The Journal of Investigative Dermatology|August 1, 1994
Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9qJ G Compton, A M Goldstein, M Turner, et al.
Human Genetics|December 18, 1998
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratodermaG Richard, T W White, L E Smith, et al.
Nature Genetics|March 1, 1995
Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosisL J Russell, J J DiGiovanna, G R Rogers, et al.
The Journal of Investigative Dermatology|January 1, 1994
Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosisJ M Yang, C C Chipev, J J DiGiovanna, et al.
The Journal of Investigative Dermatology|September 1, 1995
Hailey-Hailey disease maps to a 5 cM interval on chromosome 3q21-q24G Richard, B P Korge, A R Wright, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Regulatory sequences involved in the hormonal control of casein gene expressionJ M Rosen, W K Jones, J R Rodgers, et al.
The Journal of Experimental Zoology|August 1, 1992
Genetic linkage analysis of the murine developmental mutant velvet coat (Ve) and the distal chromosome 15 developmental genes Hox-3.1, Rar-g, Wnt-1, and Krt-2C P Hart, J G Compton, S H Langley, et al.
Nature Genetics|January 1, 1996
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneV De Laurenzi, G R Rogers, D J Hamrock, et al.
Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
The Journal of Investigative Dermatology|February 11, 1998
A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral alleleT N Darling, B B Koh, S J Bale, et al.
The Journal of Investigative Dermatology|August 1, 1994
Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9qJ G Compton, A M Goldstein, M Turner, et al.
Human Genetics|December 18, 1998
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratodermaG Richard, T W White, L E Smith, et al.
Nature Genetics|March 1, 1995
Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosisL J Russell, J J DiGiovanna, G R Rogers, et al.
The Journal of Investigative Dermatology|January 1, 1994
Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosisJ M Yang, C C Chipev, J J DiGiovanna, et al.
The Journal of Investigative Dermatology|September 1, 1995
Hailey-Hailey disease maps to a 5 cM interval on chromosome 3q21-q24G Richard, B P Korge, A R Wright, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Regulatory sequences involved in the hormonal control of casein gene expressionJ M Rosen, W K Jones, J R Rodgers, et al.
The Journal of Experimental Zoology|August 1, 1992
Genetic linkage analysis of the murine developmental mutant velvet coat (Ve) and the distal chromosome 15 developmental genes Hox-3.1, Rar-g, Wnt-1, and Krt-2C P Hart, J G Compton, S H Langley, et al.
Nature Genetics|January 1, 1996
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneV De Laurenzi, G R Rogers, D J Hamrock, et al.
Nature Genetics|December 8, 1998
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilisG Richard, L E Smith, R A Bailey, et al.
Pageof 5