학술논문

A microdeletion on Xq22.1 in a girl with developmental delay and epilepsy may help define a critical region of pathogenicity
Document Type
Journal
Source
EUROPEAN JOURNAL OF HUMAN GENETICS; APR 2022, 30 SUPPL 1, p369-p370, 2p. Supplement: 1
Subject
Language
English
ISSN
14765438