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PMID: 11584295 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Segmental duplications: an 'expanding' role in genomic instability and disease.

Nature reviews. Genetics ·Vol. 2 ·No. 10 ·2001-10-00 ·Pages 791-800

Emanuel BS, Shaikh TH

Abstract

The knowledge that specific genetic diseases are caused by recurrent chromosomal aberrations has indicated that genomic instability might be directly related to the structure of the regions involved. The sequencing of the human genome has directed significant attention towards understanding the molecular basis of such recombination 'hot spots'. Segmental duplications have emerged as a significant factor in the aetiology of disorders that are caused by abnormal gene dosage. These observations bring us closer to understanding the mechanisms and consequences of genomic rearrangement.

MeSH Terms
Angelman Syndrome/genetics Charcot-Marie-Tooth Disease/genetics Chromosome Aberrations Chromosomes, Human/genetics,ultrastructure Gene Deletion Gene Dosage Gene Duplication Genetic Diseases, Inborn/genetics Hereditary Sensory and Motor Neuropathy/genetics Humans Prader-Willi Syndrome/genetics Recombination, Genetic Repetitive Sequences, Nucleic Acid Translocation, Genetic
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Emanuel B S
Division of Human Genetics and Molecular Biology, 1002 Abramson Research Center, The Children's Hospital of Philadelphia, 3516 Civic Center Blvd, Philadelphia, Pennsylvania 19104, USA. beverly@mail.med.upenn.edu
Shaikh T H
Article Info
Journal
Nature reviews. Genetics
Abbr.
Nat Rev Genet
ISSN
1471-0056
Published
2001-10-00
Pages
791-800
Language
English
Region
England
NLM ID
100962779
Subset
IM
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