A CGH array study in nonsyndromic (primary) autism patients: deletions on 16p13.11, 16p11.2, 1q21.1, 2q21.1q21.2, and 8p23.1
TURKISH JOURNAL OF MEDICAL SCIENCES, vol.45, no.2, pp.313-319, 2015 (Journal Indexed in SCI)
Article / Article
Title of Journal :
TURKISH JOURNAL OF MEDICAL SCIENCES
Background/aim: To detect specific molecular changes of DNA level in primary autism patients by using whole genome CGH array technology.