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Bernard-Soulier syndrome in Pakistan: Biochemical and molecular analyses leading to identification of a novel mutation in GP1BA.
Böckelmann, D; Naz, A; Siddiqi, M Y J; Lerner, E; Sandrock-Lang, K; Shamsi, T S; Zieger, B.
Afiliación
  • Böckelmann D; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Naz A; National Institute of Blood Disease & Bone Marrow Transplantation, Karachi, Pakistan.
  • Siddiqi MYJ; National Institute of Blood Disease & Bone Marrow Transplantation, Karachi, Pakistan.
  • Lerner E; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Sandrock-Lang K; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Shamsi TS; National Institute of Blood Disease & Bone Marrow Transplantation, Karachi, Pakistan.
  • Zieger B; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Haemophilia ; 24(1): e18-e22, 2018 01.
Article en En | MEDLINE | ID: mdl-29119711
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Bernard-Soulier / Complejo GPIb-IX de Glicoproteína Plaquetaria / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Bernard-Soulier / Complejo GPIb-IX de Glicoproteína Plaquetaria / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania