Ionizing radiation and genetic risks. XVII. Formation mechanisms underlying naturally occurring DNA deletions in the human genome and their potential relevance for bridging the gap between induced DNA double-strand breaks and deletions in irradiated germ cells-Reference-Cited by-同舟云学术

Ionizing radiation and genetic risks. XVII. Formation mechanisms underlying naturally occurring DNA deletions in the human genome and their potential relevance for bridging the gap between induced DNA double-strand breaks and deletions in irradiated germ cells

Published:2013-10 Issue:2 Volume:753 Page:114-130
ISSN:1383-5742
Container-title:Mutation Research/Reviews in Mutation Research
language:en
Short-container-title:Mutation Research/Reviews in Mutation Research

Author:

Sankaranarayanan Krishnaswami,Taleei Reza,Rahmanian Shirin,Nikjoo Hooshang

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference197 articles.

1. Mutation induction in mice;Searle;Adv. Radiat. Biol.,1974

2. Radiation genetics;Wolff;Annu. Rev. Genet.,1967

3. Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse;Cattanach;Nat. Genet.,1993

4. Incidence and distribution of radiation-induced large deletions in the mouse;Cattanach,1996

5. Fine structure mapping and deletion analysis of the murine piebald locus;Metallinos;Genetics,1994

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