Rare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases

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YAKUT UZUNER S., Cetin Z., ŞİMŞEK M., MENDİLCİOĞLU İ. İ., TORU H. S., Berker Karauzum S., ...Daha Fazla

TURKISH JOURNAL OF PATHOLOGY, cilt.31, sa.1, ss.36-44, 2015 (ESCI)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 31 Sayı: 1
  • Basım Tarihi: 2015
  • Doi Numarası: 10.5146/tjpath.2014.01280
  • Dergi Adı: TURKISH JOURNAL OF PATHOLOGY
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.36-44
  • Anahtar Kelimeler: Prenatal diagnosis, Cytogenetics, Chromosomal aberrations, Autopsy, INCREASED NUCHAL TRANSLUCENCY, OF-THE-LITERATURE, RING CHROMOSOME-21, MOLECULAR CHARACTERIZATION, PROXIMAL 15Q, MONOSOMY, 18P, DELETION, TRANSLOCATION, EUROPE
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Akdeniz Üniversitesi Adresli: Evet

Özet

Objective: The aim of this study was presentation of the ultrasonographic findings and perinatal autopsy of cases with rare chromosomal abnormalities.