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G H S Ashton

Showing results (1-10 of 11) with videos related to

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Clinical and Experimental Dermatology|February 28, 2004
Kindler syndromeG H S Ashton
Clinical and Experimental Dermatology|February 24, 2005
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twinsH Fassihi, G H S Ashton, J Denyer, et al.
Clinical and Experimental Dermatology|November 29, 2005
Retrospective diagnosis of Kindler syndrome in a 37-year-old manM A Thomson, G H S Ashton, J A McGrath, et al.
The British Journal of Dermatology|November 18, 2003
Dilemmas in distinguishing between dominant and recessive forms of dystrophic epidermolysis bullosaR Mallipeddi, O Bleck, J E Mellerio, et al.
Clinical and Experimental Dermatology|April 6, 2005
An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 geneG Sethuraman, H Fassihi, G H S Ashton, et al.
Clinical and Experimental Dermatology|March 26, 2003
Fish odour syndrome with features of both primary and secondary trimethylaminuriaE A Fraser-Andrews, N J Manning, G H S Ashton, et al.
Clinical and Experimental Dermatology|January 25, 2005
Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosaH Fassihi, V Wessagowit, G H S Ashton, et al.
Experimental Dermatology|May 8, 2002
Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1T Hamada, A P South, Y Mitsuhashi, et al.
The British Journal of Dermatology|March 21, 2002
Human Ro60 (SSA2) genomic organization and sequence alterations, examined in cutaneous lupus erythematosusT P Millard, G H S Ashton, E Kondeatis, et al.
The British Journal of Dermatology|March 21, 2002
EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosisA P South, G H S Ashton, C Willoughby, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinical and Experimental Dermatology|February 28, 2004
Kindler syndromeG H S Ashton
Clinical and Experimental Dermatology|February 24, 2005
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twinsH Fassihi, G H S Ashton, J Denyer, et al.
Clinical and Experimental Dermatology|November 29, 2005
Retrospective diagnosis of Kindler syndrome in a 37-year-old manM A Thomson, G H S Ashton, J A McGrath, et al.
The British Journal of Dermatology|November 18, 2003
Dilemmas in distinguishing between dominant and recessive forms of dystrophic epidermolysis bullosaR Mallipeddi, O Bleck, J E Mellerio, et al.
Clinical and Experimental Dermatology|April 6, 2005
An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 geneG Sethuraman, H Fassihi, G H S Ashton, et al.
Clinical and Experimental Dermatology|March 26, 2003
Fish odour syndrome with features of both primary and secondary trimethylaminuriaE A Fraser-Andrews, N J Manning, G H S Ashton, et al.
Clinical and Experimental Dermatology|January 25, 2005
Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosaH Fassihi, V Wessagowit, G H S Ashton, et al.
Experimental Dermatology|May 8, 2002
Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1T Hamada, A P South, Y Mitsuhashi, et al.
The British Journal of Dermatology|March 21, 2002
Human Ro60 (SSA2) genomic organization and sequence alterations, examined in cutaneous lupus erythematosusT P Millard, G H S Ashton, E Kondeatis, et al.
The British Journal of Dermatology|March 21, 2002
EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosisA P South, G H S Ashton, C Willoughby, et al.
Pageof 2