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., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES, cilt.45, ss.313-319, 2015 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 45 Konu: 2
  • Basım Tarihi: 2015
  • Doi Numarası: 10.3906/sag-1310-81
  • Dergi Adı: TURKISH JOURNAL OF MEDICAL SCIENCES
  • Sayfa Sayısı: ss.313-319

Özet

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