HANHART SYNDROME

Dogan D. G., Dogan M., Aslan M., Menekse E., Yakinci C.

GENETIC COUNSELING, cilt.21, sa.4, ss.359-362, 2010 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 21 Sayı: 4
  • Basım Tarihi: 2010
  • Dergi Adı: GENETIC COUNSELING
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.359-362
  • İnönü Üniversitesi Adresli: Evet

Özet

Hanhart syndrome: We report on a male infant with Hanhart Syndrome. It is classified in "oromandibular limb hypogenesis syndromes" which are a group of rare conditions involving congenital malformations of tongue, mandible, and limbs.