Other genomic disorders and congenital heart disease
Author:
Affiliation:
1. Department of Molecular and Human GeneticsBaylor College of Medicine Houston Texas
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31762
Reference110 articles.
1. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
2. Transcription factor COUP-TFII is indispensable for venous and lymphatic development in zebrafish and Xenopus laevis
3. Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities
4. Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort
5. 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families
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