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David McGibbon

Showing results (1-10 of 8) with videos related to

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Transactions of the Medical Society of London|May 30, 2015
Diagnosis of skin diseases old and newDavid McGibbon
Orphanet Journal of Rare Diseases|November 3, 2011
Xeroderma pigmentosumAlan R Lehmann, David McGibbon, Miria Stefanini
Arthritis and Rheumatism|June 30, 2005
Lack of support for the presence of an osteoarthritis susceptibility locus on chromosome 6pGary K Meenagh, David McGibbon, James Nixon, et al.
Lupus|May 31, 2022
Proton pump inhibitor induced subacute cutaneous lupus erythematosus: Clinical characteristics and outcomesYih Jia Poh, Abdulrahman Alrashid, Shirish R Sangle, et al.
The Journal of Investigative Dermatology|January 9, 2016
A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/AfghanistanMieran Sethi, Shaheen Haque, Heather Fawcett, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Retinal vein occlusion, homocysteine, and methylene tetrahydrofolate reductase genotypeStuart J McGimpsey, Jayne V Woodside, Louise Bamford, et al.
American Journal of Human Genetics|April 30, 2013
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaKazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 18, 2016
Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defectHiva Fassihi, Mieran Sethi, Heather Fawcett, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Transactions of the Medical Society of London|May 30, 2015
Diagnosis of skin diseases old and newDavid McGibbon
Orphanet Journal of Rare Diseases|November 3, 2011
Xeroderma pigmentosumAlan R Lehmann, David McGibbon, Miria Stefanini
Arthritis and Rheumatism|June 30, 2005
Lack of support for the presence of an osteoarthritis susceptibility locus on chromosome 6pGary K Meenagh, David McGibbon, James Nixon, et al.
Lupus|May 31, 2022
Proton pump inhibitor induced subacute cutaneous lupus erythematosus: Clinical characteristics and outcomesYih Jia Poh, Abdulrahman Alrashid, Shirish R Sangle, et al.
The Journal of Investigative Dermatology|January 9, 2016
A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/AfghanistanMieran Sethi, Shaheen Haque, Heather Fawcett, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Retinal vein occlusion, homocysteine, and methylene tetrahydrofolate reductase genotypeStuart J McGimpsey, Jayne V Woodside, Louise Bamford, et al.
American Journal of Human Genetics|April 30, 2013
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaKazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 18, 2016
Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defectHiva Fassihi, Mieran Sethi, Heather Fawcett, et al.
Pageof 1