Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans-Reference-Cited by-同舟云学术

Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans

Published:2006-05 Issue:5 Volume:78 Page:878-883
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Gilling Mette,Dullinger Jörn S.,Gesk Stefan,Metzke-Heidemann Simone,Siebert Reiner,Meyer Thomas,Brondum-Nielsen Karen,Tommerup Niels,Ropers Hans-Hilger,Tümer Zeynep,Kalscheuer Vera M.,Thomas N. Simon

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Chromosome abnormalities and genetic counselling;Gardner,1996

2. Inv(10)(p11.2q21.2), a variant chromosome;Collinson;Hum Genet,1997

3. Pericentric inversions in man: a French collaborative study;Goupe de Cytogénéticiens Français;Ann Genet,1986

4. Segregation analysis of balanced pericentric inversions in pedigree data;Sherman;Clin Genet,1986

5. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories;Daniel;Am J Med Genet,1989

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