A novel deletion involving exon 13 of factor VIII gene in a newborn with splenic hematoma.

Gurlek Gokcebay, Dilek; Akpinar Tekgunduz, Sibel; Sarici, Dilek; Uysal Ramadan, Selma; Cavdarli, Busranur

Gurlek Gokcebay, Dilek; Akpinar Tekgunduz, Sibel; Sarici, Dilek; Uysal Ramadan, Selma; Cavdarli, Busranur.

Afiliación

Gurlek Gokcebay D; Department of Pediatric Hematology, University of Health Sciences Kecioren Training and Research Hospital, Turkey. Electronic address: drdilekgurlek@hotmail.com.
Akpinar Tekgunduz S; Department of Pediatric Hematology, University of Health Sciences Kecioren Training and Research Hospital, Turkey.
Sarici D; Department of Neonatology, University of Health Sciences Kecioren Training and Research Hospital, Turkey.
Uysal Ramadan S; Department of Radiology, University of Health Sciences Kecioren Training and Research Hospital, Turkey.
Cavdarli B; Department of Medical Genetics, University of Health Sciences Ankara Numune Training and Research Hospital, Turkey.

Transfus Apher Sci ; 59(1): 102562, 2020 Feb.

Article en En | MEDLINE | ID: mdl-31230948

Asunto(s)

Exones/genética; Factor VIII/metabolismo; Hematoma/sangre; Eliminación de Secuencia/genética; Rotura del Bazo/sangre; Humanos; Recién Nacido; Masculino

Palabras clave

Deletion; Hemophilia; Newborn; Splenic hematoma

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rotura del Bazo / Factor VIII / Exones / Eliminación de Secuencia / Hematoma Límite: Humans / Male / Newborn Idioma: En Revista: Transfus Apher Sci Asunto de la revista: HEMATOLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Reino Unido

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