Familial mutation in caffey disease with reduced penetrance: a case report-Reference-Cited by-同舟云学术

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Familial mutation in caffey disease with reduced penetrance: a case report

Published:2016 Issue:6 Volume:58 Page:650
ISSN:0041-4301
Container-title:The Turkish Journal of Pediatrics
language:
Short-container-title:TurkJPediatr

Author:

Özdemir Özmert M.A.,Tancer-Elçi Hazal,Polat Aziz,Güçtürk İnci,Tepeli Emre,Zeybek Selcan,Ayaz Akif

Publisher

The Turkish Journal of Pediatrics

Subject

Pediatrics, Perinatology and Child Health

Cited by 2 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. Expanding the Clinical Spectrum of Osteogenesis Imperfecta Type V: 13 Additional Patients and Review;Frontiers in Endocrinology;2019-06-12

2. Unusual findings on infantile cortical hyperostosis: A case report;Special Care in Dentistry;2018-06-29

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