The Comet Assay as a Repair Test for Prenatal Diagnosis of Xeroderma Pigmentosum and Trichothiodystrophy

Author:

Alapetite Claire,Benoit Annie,Moustacchi Ethel,Sarasin Alain

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference22 articles.

1. Use of the alkaline comet assay to detect DNA repair deficiencies in human fibrobolasts exposed to UVC, UVB, UVA and gamma-rays;Alapetite;Int J Radiat Biol,1996

2. Prenatal exclusion of xeroderma pigmentosum (XP-D) by amniotic cell analysis;Arase;Photodermatol,1985

3. Nucleotide excision repair syndromes: molecular basis and clinical symptoms;Bootsma;Philos Trans R Soc Lond [Biol],1995

4. Defective repair replication of DNA in xeroderma pigmentosum;Cleaver;Nature,1968

5. Prenatal diagnosis of xeroderma pigmentosum and Cockayne syndrome;Cleaver;Prenat Diagn,1994

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