Whole exome sequencing identifies de novo mutations inGATA6associated with congenital diaphragmatic hernia

First report of a de novo 18q11.2 microdeletion including GATA6 associated with complex congenital heart disease and renal abnormalities

(2013) Peter H. Bui et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Congenital absence of the pericardium and its mimics

(2013) Franco Verde et al.   Journal of Cardiovascular Computed Tomography

GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

(2012) E. De Franco et al.   DIABETES

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

(2012) Lan Yu et al.   HUMAN GENETICS

De novo copy number variants are associated with congenital diaphragmatic hernia

(2012) Lan Yu et al.   JOURNAL OF MEDICAL GENETICS

De novo mutations in human genetic disease

(2012) Joris A. Veltman et al.   NATURE REVIEWS GENETICS

Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes

(2012) M. K. Russell et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

(2012) B. J. O'Roak et al.   SCIENCE

Congenital absence of the left pericardium and diaphragmatic defect in sibs

(2010) Alain Verloes et al.   European Journal of Medical Genetics

Genetic aspects of human congenital diaphragmatic hernia

(2009) BR Pober   CLINICAL GENETICS

Crystal Structures of Multiple GATA Zinc Fingers Bound to DNA Reveal New Insights into DNA Recognition and Self-Association by GATA

(2008) Darren L. Bates et al.   JOURNAL OF MOLECULAR BIOLOGY

A Gata6-Wnt pathway required for epithelial stem cell development and airway regeneration

(2008) Yuzhen Zhang et al.   NATURE GENETICS