Delineation of the Critical Deletion Region for Congenital Heart Defects, on Chromosome 8p23.1
- 1 April 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (4) , 1119-1126
- https://doi.org/10.1086/302330
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Sex–dependent rearrangements resulting in CMT1A and HNPPNature Genetics, 1997
- Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis.Genes & Development, 1997
- GATA4 transcription factor is required for ventral morphogenesis and heart tube formation.Genes & Development, 1997
- A complete set of human telomeric probes and their clinical applicationNature Genetics, 1996
- Distal 8p deletion (8)(p23.1): An easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardationAmerican Journal of Medical Genetics, 1996
- Assignment of the human GATA4 gene to 8p23.1→p22 using fluorescence in situ hybridization analysisCytogenetic and Genome Research, 1996
- Assignment of the human glypican gene (GPC1) to 2q35–q37 by fluorescence in situ hybridizationGenomics, 1995
- Atrioventricular canal and 8p‐ syndromeAmerican Journal of Medical Genetics, 1993
- Nonrandom association of atrioventricular canal and del (8p) syndromeAmerican Journal of Medical Genetics, 1992
- Deficiency of chromosome 8p21.1→8pter: Case report and review of the literatureAmerican Journal of Medical Genetics, 1985