Down syndrome congenital heart disease: A narrowed region and a candidate gene
- 1 March 2001
- journal article
- case report
- Published by Elsevier in Genetics in Medicine
- Vol. 3 (2) , 91-101
- https://doi.org/10.1097/00125817-200103000-00002
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Down Syndrome Critical Region Gene 2: Expression during Mouse Development and in Human Cell Lines Indicates a Function Related to Cell ProliferationBiochemical and Biophysical Research Communications, 2000
- Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3Human Genetics, 1997
- BAC and PAC Contigs Covering 3.5 Mb of the Down Syndrome Congenital Heart Disease Region between D21S55 and MX1 on Chromosome 21Genomics, 1997
- Cloning of a Human Homolog of theDrosophila Minibrain/Rat Dyrk Gene from “the Down Syndrome Critical Region” of Chromosome 21Biochemical and Biophysical Research Communications, 1996
- Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridizationCytogenetic and Genome Research, 1995
- Simplifying the understanding of congenital malformations of the heartInternational Journal of Cardiology, 1991
- Expression of adhesion molecules during the formation and differentiation of the avian endocardial cushion tissueDevelopmental Biology, 1991
- Induction of an epithelial-mesenchymal transition by an in vivo adheron-like complexDevelopmental Biology, 1989
- Pulmonary Hypoplasia in Down's SyndromeNew England Journal of Medicine, 1982
- Clinical diagnosis of Down's syndromeClinical Genetics, 1976