Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1

Devriendt, K, Matthijs, G, Van Dael, R, Gewillig, M, Eyskens, B, Hjalgrim, H, Dolmer, B, McGaughran, J, Brondum-Nielsen, K, Marynen, P, Fryns, JP and Vermeesch, JR (1999) Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. American Journal of Human Genetics, 64 4: 1119-1126. doi:10.1086/302330


Author Devriendt, K
Matthijs, G
Van Dael, R
Gewillig, M
Eyskens, B
Hjalgrim, H
Dolmer, B
McGaughran, J
Brondum-Nielsen, K
Marynen, P
Fryns, JP
Vermeesch, JR
Title Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
Journal name American Journal of Human Genetics   Check publisher's open access policy
ISSN 0002-9297
Publication date 1999-04-01
Year available 1999
Sub-type Article (original research)
DOI 10.1086/302330
Open Access Status Not Open Access
Volume 64
Issue 4
Start page 1119
End page 1126
Total pages 8
Publisher UNIV CHICAGO PRESS
Language eng
Keyword In-Situ Hybridization
Ventral Morphogenesis
Insitu Hybridization
Transcription Factor
Mental-Retardation
Tube Formation
8p Syndrome
Short Arm
Disease
Gata4
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: ResearcherID Downloads - Archived
 
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