학술논문
Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome
Document Type
Article
Author
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, 2019, 179(9):1783-1790)
Subject
Language
English
ISSN
15524833
15524825
15524825