학술논문
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function
Document Type
Article
Source
In: Journal of Medical Genetics . (Journal of Medical Genetics, 1 July 2023, 60(7):712-716)
Subject
Language
English
ISSN
14686244
00222593
00222593