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1.
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
Am J Hum Genet
; 92(5): 807-19, 2013 May 02.
Article
in English
| MEDLINE | ID: mdl-23623389
2.
Neurological symptoms and natural course of xeroderma pigmentosum.
Brain
; 131(Pt 8): 1979-89, 2008 Aug.
Article
in English
| MEDLINE | ID: mdl-18567921
3.
Translesion synthesis: Y-family polymerases and the polymerase switch.
DNA Repair (Amst)
; 6(7): 891-9, 2007 Jul 01.
Article
in English
| MEDLINE | ID: mdl-17363342
4.
A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/Afghanistan.
J Invest Dermatol
; 136(4): 869-872, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26743599
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