Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects-Reference-Cited by-同舟云学术

Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects

Published:2013-05-21 Issue:7 Volume:161 Page:1755-1758
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Keitges Elisabeth A.¹,Pasion Romela²,Burnside Rachel D.²,Mason Carla³,Gonzalez-Ruiz Antonio³,Dunn Teresa⁴,Masiello Meredith⁴,Gebbia Joseph A.⁴,Fernandez Carlos O.⁵,Risheg Hiba¹

Affiliation:

1. Department of Cytogenetics; Laboratory Corporation of America/Dynacare; Seattle, Washington

2. Department of Cytogenetics; Laboratory Corporation of America, Center for Molecular Biology and Pathology; Research Triangle Park, North Carolina

3. Brookwood Maternal Fetal Medicine; Birmingham, Alabama

4. Medical Genetic Testing Laboratories; CytoGenX Corp.; Stony Brook, New York

5. Premiere Perinatal, LLC; Toms River, New Jersey

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects;Jay;Dev Biol,2007

2. GATA4 transcription factor is required for ventral morphogenesis and heart tube formation;Kuo;Genes Dev,1997

3. Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities;Lalani;Eur J Hum Genet,2013

4. Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks;Longoni;Am J Med Genet Part A,2012

5. Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis;Molkentin;Genes Dev,1997

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