[Phenotypic and genotypic analysis of a fetus carrying an intermediate 22q11.2 deletion encompassing the CRKL gene].
Year: 2017
Type: article
Study design: Case Report
Source: PubMed
Authors: Shaobin Lin, Xiaohe Zheng, Heng Gu, Mingzhen Li
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2991097793
