학술논문
Homozygous variant in C21orf2 in a case of Jeune syndrome with severe thoracic involvement: Extending the phenotypic spectrum
Document Type
Article
Author
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, June 2017, 173(6):1698-1704)
Subject
Language
English
ISSN
15524833
15524825
15524825