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Interstitial 3p25.3 deletion syndrome: 13 years'-long follow-up of an affected individual.
Kocagil, Sinem; Susam, Ezgi; Yimenicioglu, Sevgi; Aynaci, Sabri; Gökalp, Ebru Erzurumluoglu; Artan, Sevilhan.
Afiliação
  • Kocagil S; Department of Medical Genetics, Eskisehir Osmangazi University, Eskisehir.
  • Susam E; Department of Medical Genetics, Sakarya Training and Research Hospital, Sakarya.
  • Yimenicioglu S; Department of Pediatric Neurology, Eskisehir City Hospital, Eskisehir, Turkey.
  • Aynaci S; Department of Medical Genetics, Eskisehir Osmangazi University, Eskisehir.
  • Gökalp EE; Department of Medical Genetics, Eskisehir Osmangazi University, Eskisehir.
  • Artan S; Department of Medical Genetics, Eskisehir Osmangazi University, Eskisehir.
Clin Dysmorphol ; 2024 May 21.
Article em En | MEDLINE | ID: mdl-38856647

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article