Work

Mutation Analysis of FGFR1-3 in 11 Japanese Patients with Syndromic Craniosynostosis

Year: 2016

Type: article

Source: The Japanese Society for Pediatric Endocrinology

Author: 加藤芙弥子

Language: English

Topic: Craniofacial Disorders and Treatments

Subfield: Surgery

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2760787902

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Related to: 10