학술논문
De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndrome
Document Type
Article
Author
Source
In: European Journal of Medical Genetics . (European Journal of Medical Genetics, July 2010, 53(4):208-212)
Subject
Language
English
ISSN
17697212