Use of targeted next-generation sequencing for molecular diagnosis of craniosynostosis: Identification of a novelde novomutation ofEFNB1-Reference-Cited by-同舟云学术

Use of targeted next-generation sequencing for molecular diagnosis of craniosynostosis: Identification of a novelde novomutation ofEFNB1

Author:

Yamamoto Toshiyuki¹,Igarashi Naru²,Shimojima Keiko¹,Sangu Noriko¹,Sakamoto Yuko³,Shimoji Kazuaki⁴,Niijima Shinichi²

Affiliation:

1. Tokyo Women's Medical University Institute for Integrated Medical Sciences; Tokyo Japan

2. Department of Pediatrics; Juntendo University Nerima Hospital; Tokyo Japan

3. Department of Orthopedics; Juntendo University Nerima Hospital; Tokyo Japan

4. Department of Neurosurgery; Juntendo University; Tokyo Japan

Funder

Ministry of Health, Labor, and Welfare, Japan

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

Reference30 articles.

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

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