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A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant.
Deliloglu, Burak; Tüfekçi, Özlem; Tüzün, Funda; Aykut, Ayça; Ceylan, Emine Ipek; Durmaz, Asude; Yilmaz, Sebnem; Duman, Nuray; Özkan, Hasan; Ören, Hale.
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  • Deliloglu B; Department of Pediatrics, Divisions of Neonatology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
  • Tüfekçi Ö; Department of Pediatric Hematology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
  • Tüzün F; Department of Pediatrics, Divisions of Neonatology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
  • Aykut A; Department of Medical Genetics, Ege University Faculty of Medicine, Izmir, Turkey.
  • Ceylan EI; Department of Medical Genetics, Ege University Faculty of Medicine, Izmir, Turkey.
  • Durmaz A; Department of Medical Genetics, Ege University Faculty of Medicine, Izmir, Turkey.
  • Yilmaz S; Department of Pediatric Hematology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
  • Duman N; Department of Pediatrics, Divisions of Neonatology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
  • Özkan H; Department of Pediatrics, Divisions of Neonatology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
  • Ören H; Department of Pediatric Hematology, Dokuz Eylul University Faculty of Medine, Izmir, Turkey.
Turk J Pediatr ; 64(4): 736-740, 2022.
Article en En | MEDLINE | ID: mdl-36082647
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trombocitopenia Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Turk J Pediatr Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trombocitopenia Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Turk J Pediatr Año: 2022 Tipo del documento: Article