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The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review.
Karamik, Gokcen; Tuysuz, Beyhan; Isik, Esra; Yilmaz, Aysegul; Alanay, Yasemin; Sunamak, Evrim Cifci; Durmusalioglu, Enise Avci; Ozkinay, Ferda; Cetin, Gokhan Ozan; Ozturk, Nuray; Mihci, Ercan; Nur, Banu.
Afiliação
  • Karamik G; Department of Pediatrics, Division of Pediatric Genetics, Akdeniz University, Antalya, Turkey.
  • Tuysuz B; Department of Pediatrics, Division of Pediatric Genetics, Cerrahpasa University, Istanbul, Turkey.
  • Isik E; Department of Pediatrics, Division of Pediatric Genetics, Ege University, Izmir, Turkey.
  • Yilmaz A; Department of Pediatrics, Division of Pediatric Genetics, Ondokuz Mayis University, Samsun, Turkey.
  • Alanay Y; Department of Pediatrics, Division of Pediatric Genetics, Acibadem University, Istanbul, Turkey.
  • Sunamak EC; Department of Pediatrics, Division of Pediatric Genetics, Cerrahpasa University, Istanbul, Turkey.
  • Durmusalioglu EA; Department of Pediatrics, Division of Pediatric Genetics, Ege University, Izmir, Turkey.
  • Ozkinay F; Department of Pediatrics, Division of Pediatric Genetics, Ege University, Izmir, Turkey.
  • Cetin GO; Department of Medical Genetics, Pamukkale University, Denizli, Turkey.
  • Ozturk N; Department of Pediatrics, Division of Pediatric Genetics, Akdeniz University, Antalya, Turkey.
  • Mihci E; Department of Pediatrics, Division of Pediatric Genetics, Akdeniz University, Antalya, Turkey.
  • Nur B; Department of Pediatrics, Division of Pediatric Genetics, Akdeniz University, Antalya, Turkey.
Am J Med Genet A ; 191(7): 1814-1825, 2023 07.
Article em En | MEDLINE | ID: mdl-37053206

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Deficiência Intelectual Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Deficiência Intelectual Idioma: En Ano de publicação: 2023 Tipo de documento: Article