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., ...Daha Fazla

TURKISH JOURNAL OF MEDICAL SCIENCES, cilt.45, sa.2, ss.313-319, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45 Sayı: 2
  • Basım Tarihi: 2015
  • Doi Numarası: 10.3906/sag-1310-81
  • Dergi Adı: TURKISH JOURNAL OF MEDICAL SCIENCES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.313-319
  • Anahtar Kelimeler: Autism spectrum disorders, primary autism, CGH-array, deletion, COMPARATIVE GENOMIC HYBRIDIZATION, COPY NUMBER VARIATIONS, SPECTRUM DISORDERS, TWIN PAIRS, GENETICS
  • Kocaeli Üniversitesi Adresli: Evet

Özet

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