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PMID: 15060116 Published · ppublish English Letter Research Support, Non-U.S. Gov't

Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients.

Journal of medical genetics ·Vol. 41 ·No. 4 ·2004-04-00 ·Pages e40

Rauch A, Devriendt K, Koch A, Rauch R, Gewillig M, Kraus C, Weyand M, Singer H, Reis A, Hofbeck M

Abstract

暂无摘要

MeSH Terms

Chromosome Deletion Chromosomes, Human, Pair 22 Genetic Predisposition to Disease Haplotypes Heart Defects, Congenital/diagnosis,genetics Humans Linkage Disequilibrium Mutation Polymorphism, Single Nucleotide T-Box Domain Proteins/genetics

Chemicals

T-Box Domain Proteins TBX1 protein, human

Authors & Affiliations

10 authors, click to expand affiliations / ORCID

Rauch A

Devriendt K

Koch A

Rauch R

Gewillig M

Kraus C

Weyand M

Singer H

Reis A

Hofbeck M

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

1468-6244

DOI

10.1136/jmg.2003.010975

Published

2004-04-00

Pages

e40

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1735727

Subset

External Links

PubMed source DOI: 10.1136/jmg.2003.010975 PMC Full Text View journal details

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Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients.

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