Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

Title
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 149A, Issue 8, Pages 1661-1677
Publisher
Wiley
Online
2009-07-18
DOI
10.1002/ajmg.a.32896

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