Additional EFNB1 mutations in craniofrontonasal syndrome

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Bibliographic Details
Published in:	American journal of medical genetics. Part A Vol. 146A; no. 15; pp. 2008 - 2012
Main Authors:	Wallis, Deeann, Lacbawan, Felicitas, Jain, Mahim, Der Kaloustian, Vazken M., Steiner, Carlos E., Moeschler, John B., Losken, H. Wolfgang, Kaitila, Ilkka I., Cantrell, Stephen, Proud, Virginia K., Carey, John C., Day, Donald W., Lev, Dorit, Teebi, Ahmad S., Robinson, Luther K., Hoyme, H. Eugene, Al-Torki, Nadia, Siegel-Bartelt, Jacqueline, Mulliken, John B., Robin, Nathaniel H., Saavedra, Dolores, Zackai, Elaine H., Muenke, Maximilian
Format:	Journal Article
Language:	English
Published:	Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-08-2008 Wiley-Liss
Subjects:	Biological and medical sciences Chromosomes, Human, X Craniosynostoses - genetics DNA - genetics Ephrin-B1 - genetics Female Humans Male Medical genetics Medical sciences Mutation Polymerase Chain Reaction Sequence Analysis, DNA Syndrome Mutation Crâniofrontonasal syndrome Complex syndrome Malformation
Online Access:	Get full text
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