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Blended Phenotype of Pelger-Huet Anomaly with Osteochondroma and Autosomal Recessive Deafness with Enlarged Vestibular Aqueduct.
Cinleti, Tayfun; Yilmaz Uzman, Ceren; Akyol, Sefika; Tüfekçi, Özlem; Erçal, Murat Derya; Giray Bozkaya, Özlem.
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  • Cinleti T; Branch of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Yilmaz Uzman C; Branch of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Akyol S; Branch of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Tüfekçi Ö; Branch of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Erçal MD; Branch of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
  • Giray Bozkaya Ö; Branch of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey.
Mol Syndromol ; 13(3): 200-205, 2022 May.
Article en En | MEDLINE | ID: mdl-35707587
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Mol Syndromol Año: 2022 Tipo del documento: Article País de afiliación: Turquía
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Mol Syndromol Año: 2022 Tipo del documento: Article País de afiliación: Turquía