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Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X‐linked midline gene?

Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for... We report on familial occurrence of congenital diaphragmatic defect and associated midline anomalies, namely cleft palate and omphalocele in brothers. This family further supports the existence of an X‐linked gene involved in the organization of the embryonal midline. This particular mutant gene might be active in the schisis‐morphogenesis phenomena occurring at the midline. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png American Journal of Medical Genetics Part A Wiley

Familial congenital diaphragmatic defect and associated midline anomalies: Further evidence for an X‐linked midline gene?

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References (14)

Publisher
Wiley
Copyright
Copyright © 1990 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1552-4825
eISSN
1552-4833
DOI
10.1002/ajmg.1320360314
pmid
2363430
Publisher site
See Article on Publisher Site

Abstract

We report on familial occurrence of congenital diaphragmatic defect and associated midline anomalies, namely cleft palate and omphalocele in brothers. This family further supports the existence of an X‐linked gene involved in the organization of the embryonal midline. This particular mutant gene might be active in the schisis‐morphogenesis phenomena occurring at the midline.

Journal

American Journal of Medical Genetics Part AWiley

Published: Jul 1, 1990

Keywords: ; ; ;

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