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Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7.
Pastor, Victor B; Sahoo, Sushree S; Boklan, Jessica; Schwabe, Georg C; Saribeyoglu, Ebru; Strahm, Brigitte; Lebrecht, Dirk; Voss, Matthias; Bryceson, Yenan T; Erlacher, Miriam; Ehninger, Gerhard; Niewisch, Marena; Schlegelberger, Brigitte; Baumann, Irith; Achermann, John C; Shimamura, Akiko; Hochrein, Jochen; Tedgård, Ulf; Nilsson, Lars; Hasle, Henrik; Boerries, Melanie; Busch, Hauke; Niemeyer, Charlotte M; Wlodarski, Marcin W.
Afiliação
  • Pastor VB; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Sahoo SS; Faculty of Biology, University of Freiburg, Germany.
  • Boklan J; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Schwabe GC; Faculty of Biology, University of Freiburg, Germany.
  • Saribeyoglu E; Spemann Graduate School of Biology and Medicine, University of Freiburg, Germany.
  • Strahm B; Center for Cancer and Blood Disorders, Phoenix Children's Hospital, AZ, USA.
  • Lebrecht D; Children's Hospital, Carl-Thiem-Klinikum Cottbus, Germany.
  • Voss M; Children's Hospital, Carl-Thiem-Klinikum Cottbus, Germany.
  • Bryceson YT; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Erlacher M; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Ehninger G; Department of Medicine, Huddinge, Hematology and Regenerative Medicine, Karolinska Institute, Stockholm, Sweden.
  • Niewisch M; Department of Medicine, Huddinge, Hematology and Regenerative Medicine, Karolinska Institute, Stockholm, Sweden.
  • Schlegelberger B; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Baumann I; German Cancer Consortium (DKTK), Freiburg, Germany and German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Achermann JC; Internal Medicine of Hematology/Medical Oncology, University Hospital, Dresden, Germany.
  • Shimamura A; Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Hochrein J; Institute of Human Genetics, Hannover Medical School, Germany.
  • Tedgård U; Clinical Centre South West, Department of Pathology, Böblingen Clinics, Germany.
  • Nilsson L; Genetics & Genomic Medicine, UCL Great Ormond Street Institute of Child Health, University College London, UK.
  • Hasle H; Boston Children's Hospital, Dana Farber Cancer Institute, and Harvard Medical School, MA, USA.
  • Boerries M; Institute of Molecular Medicine and Cell Research, University of Freiburg, Germany.
  • Busch H; Department of Pediatric Oncology and Hematology, Skåne University Hospital, Lund, Sweden.
  • Niemeyer CM; Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.
  • Wlodarski MW; Department of Pediatrics, Aarhus University Hospital, Denmark.
Haematologica ; 103(3): 427-437, 2018 03.
Article em En | MEDLINE | ID: mdl-29217778
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Deleção Cromossômica / Proteínas Supressoras de Tumor Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Haematologica Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Deleção Cromossômica / Proteínas Supressoras de Tumor Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Haematologica Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha