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Cell|August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHK A Henning, L Li, N Iyer, et al.Human Molecular Genetics|December 6, 2001
Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophyV Viprakasit, R J Gibbons, B C Broughton, et al.Current Biology : CB|July 8, 1999
Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patientE Riballo, S E Critchlow, S H Teo, et al.Human Molecular Genetics|November 16, 2001
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD geneB C Broughton, M Berneburg, H Fawcett, et al.Teratogenesis, Carcinogenesis, and Mutagenesis|November 14, 2000
Molecular methods for the detection of mutationsC Monteiro, L A Marcelino, A R Conde, et al.Human Mutation|November 7, 2009
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndromeV Laugel, C Dalloz, M Durand, et al.Pageof 13