Report of a family with craniofrontonasal syndrome-Reference-Cited by-同舟云学术

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Report of a family with craniofrontonasal syndrome

Published:2015-04 Issue:2 Volume:24 Page:79-83
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Özyılmaz Berk,Gezdirici Alper,Özen Mustafa,Kalenderer Önder

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Ephrin-B1 forward signaling regulates craniofacial morphogenesis by controlling cell proliferation across Eph-ephrin boundaries.;Bush;Genes Dev,2010

2. Craniofrontonasal dysplasia.;Cohen;Birth Defects Orig Artic Ser,1979

3. A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22.;Feldman;Hum Mol Genet,1997

4. Normal periocular anthropometric measurements in the Turkish population.;Ozturk;Ophthalmic Epidemiol,2006

5. Further evidence from two families that craniofrontonasal dysplasia maps to Xp22.;Pulleyn;Clin Genet,1999

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Diagnostic value of exome and whole genome sequencing in craniosynostosis;Journal of Medical Genetics;2016-11-24

2. A Family with Craniofrontonasal Syndrome and a Mutation (p.G151S) in the EFNB1 Gene: Expanding the Phenotype;Molecular Syndromology;2016-03-19

3. Use of targeted next-generation sequencing for molecular diagnosis of craniosynostosis: Identification of a novelde novomutation ofEFNB1;Congenital Anomalies;2016-03

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