A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome

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Kılıç E., Cetinkaya A., Ütine G. E., Boduroǧlu K.

Journal of Child Neurology, cilt.31, sa.7, ss.913-917, 2016 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 31 Sayı: 7
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1177/0883073815627884
  • Dergi Adı: Journal of Child Neurology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.913-917
  • Anahtar Kelimeler: Mowat-Wilson syndrome, intellectual disability, ZEB2 gene, novel mutation, congenital anomaly, SMAD INTERACTING PROTEIN-1, HIRSCHSPRUNG-DISEASE, MUTATIONS, PHENOTYPE, SIP1, DELETIONS, SPECTRUM
  • Hacettepe Üniversitesi Adresli: Evet