Author:
Zafeiriou Dimitrios I.,Pavlidou Efterpi L.,Vargìami Euthymia
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference41 articles.
1. Center for Medical Genetics, Johns Hopkins University, and National Center for Biotechnology Information, National Library of Medicine. Online Mendelian Inheritance in Man, OMIM. 2008. Available at: http://www.ncbi.nih.gov/omim.
2. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome;Twigg;Proc Nat Acad Sci USA,2004
3. Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS);Wieland;Hum Mutat,2005
4. Craniofrontonasal dysplasia;Cohen;Birth Defects,1979
5. Expanding the phenotype of craniofrontonasal syndrome: Two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia;Vasudevan;Eur J Hum Genet,2006
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