Prenatal diagnosis of Cockayne syndrome using assay of colony-forming ability in ultraviolet light irradiated cells
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01424.x/fullpdf
Reference16 articles.
1. Cockayne's syndrome fibroblasts have increased sensitivity to ultraviolet light but normal rates of unscheduled DNA synthesis;Andrews;J. invest. Derm.,1978
2. Xeroderma pigmentosum: Biochemical and genetic characteristics;Cleaver;Ann. Rev. Genet.,1975
3. Dwarfism with retinal atrophy and deafness;Cockayne;Arch. Dis. Childh.,1936
4. The effect of changes in cell geometry on the sensitivity to ultraviolet radiation of mammalian cellular capacity;Coohill;Photochem. Photobiol.,1979
5. Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair;Halley;Clin. Genet.,1979
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2. Prenatal Diagnosis of Cockayne Syndrome Type A Based on the Identification of Two Novel Mutations in the ERCC8 Gene;Genetic Testing and Molecular Biomarkers;2009-02
3. Prenatal diagnosis of the Cockayne syndrome: survey of 15 years experience;Prenatal Diagnosis;2006
4. Ocular Manifestations in the Inherited DNA Repair Disorders;Survey of Ophthalmology;2003-01
5. The Total Amount of DNA Damage Determines Ultraviolet-radiation-induced Cytotoxicity After Uniformor Localized Irradiation of Human Cells;Journal of Investigative Dermatology;2002-11
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