Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends-Reference-Cited by-同舟云学术

Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends

Published:2003-08-18 Issue:3 Volume:22 Page:245-251
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Chuzhanova Nadia,Abeysinghe Shaun S.,Krawczak Michael,Cooper David N.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs

2. Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints

3. Palindrome resolution and recombination in the mammalian germ line

4. Homologous recombination as a mechanism for genome rearrangements: environmental and genetic effects

5. The role of DNA repeats and associated secondary structures in genomic instability and neoplasia

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