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F Capon

Showing results (21-30 of 42) with videos related to

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Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Genes and Immunity|July 10, 2009
Differential contribution of CDKAL1 variants to psoriasis, Crohn's disease and type II diabetesM Quaranta, A D Burden, C E M Griffiths, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26M Mangino, E Flex, F Capon, et al.
American Journal of Human Genetics|September 14, 2000
Mapping a dominant form of multinodular goiter to chromosome Xp22F Capon, A Tacconelli, E Giardina, et al.
Annals of Human Genetics|December 16, 2004
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 7, 2017
European consensus statement on phenotypes of pustular psoriasisA A Navarini, A D Burden, F Capon, et al.
The British Journal of Dermatology|August 15, 2009
Genetic analysis of desmoglein 3 (DSG3) sequence variants in patients with pemphigus vulgarisF Capon, H Boulding, M Quaranta, et al.
Biochemical and Biophysical Research Communications|January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5A Pizzuti, A Colosimo, A Ratti, et al.
Journal of Medical Genetics|June 3, 2004
Genetic analysis of PSORS2 markers in a UK dataset supports the association between RAPTOR SNPs and familial psoriasisF Capon, C Helms, C D Veal, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Genes and Immunity|July 10, 2009
Differential contribution of CDKAL1 variants to psoriasis, Crohn's disease and type II diabetesM Quaranta, A D Burden, C E M Griffiths, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26M Mangino, E Flex, F Capon, et al.
American Journal of Human Genetics|September 14, 2000
Mapping a dominant form of multinodular goiter to chromosome Xp22F Capon, A Tacconelli, E Giardina, et al.
Annals of Human Genetics|December 16, 2004
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locusE Giardina, F Capon, M C De Rosa, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 7, 2017
European consensus statement on phenotypes of pustular psoriasisA A Navarini, A D Burden, F Capon, et al.
The British Journal of Dermatology|August 15, 2009
Genetic analysis of desmoglein 3 (DSG3) sequence variants in patients with pemphigus vulgarisF Capon, H Boulding, M Quaranta, et al.
Biochemical and Biophysical Research Communications|January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5A Pizzuti, A Colosimo, A Ratti, et al.
Journal of Medical Genetics|June 3, 2004
Genetic analysis of PSORS2 markers in a UK dataset supports the association between RAPTOR SNPs and familial psoriasisF Capon, C Helms, C D Veal, et al.
Pageof 5