A CGH array study in nonsyndromic (primary) autism patients: deletions on 16p13.11, 16p11.2, 1q21.1, 2q21.1q21.2, and 8p23.1


Gümüşlü K., Savli H. , Sünnetçi D. , Çine N. , Kara B. , Eren K., ...More

TURKISH JOURNAL OF MEDICAL SCIENCES, vol.45, no.2, pp.313-319, 2015 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 45 Issue: 2
  • Publication Date: 2015
  • Doi Number: 10.3906/sag-1310-81
  • Title of Journal : TURKISH JOURNAL OF MEDICAL SCIENCES
  • Page Numbers: pp.313-319

Abstract

Background/aim: To detect specific molecular changes of DNA level in primary autism patients by using whole genome CGH array technology.