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
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Bibliography:	ark:/67375/WNG-GPKBX2LK-3 istex:F382D7D7816CE7DC124057855CB1A33F60542190 ArticleID:AJMG32388 This article is a US Government work and, as such, is in the public domain in the United States of America. How to cite this article: Wallis D, Lacbawan F, Jain M, Der Kaloustian VM, Steiner CE, Moeschler JB, Losken HW, Kaitila II, Cantrell S, Proud VK, Carey JC, Day DW, Lev D, Teebi AS, Robinson LK, Hoyme HE, Al-Torki N, Siegel-Bartelt J, Mulliken JB, Robin NH, Saavedra D, Zackai EH, Muenke M. 2008. Additional EFNB1 mutations in craniofrontonasal syndrome. Am J Med Genet Part A 146A:2008-2012. EFNB1 How to cite this article: Wallis D, Lacbawan F, Jain M, Der Kaloustian VM, Steiner CE, Moeschler JB, Losken HW, Kaitila II, Cantrell S, Proud VK, Carey JC, Day DW, Lev D, Teebi AS, Robinson LK, Hoyme HE, Al‐Torki N, Siegel‐Bartelt J, Mulliken JB, Robin NH, Saavedra D, Zackai EH, Muenke M. 2008. Additional mutations in craniofrontonasal syndrome. Am J Med Genet Part A 146A:2008–2012. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Deeann Wallis’s present address is Texas Institute for Genomic Medicine, Houston, TX.
ISSN:	1552-4825 1552-4833
DOI:	10.1002/ajmg.a.32388