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Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.
Muramatsu, Hideki; Okuno, Yusuke; Yoshida, Kenichi; Shiraishi, Yuichi; Doisaki, Sayoko; Narita, Atsushi; Sakaguchi, Hirotoshi; Kawashima, Nozomu; Wang, Xinan; Xu, Yinyan; Chiba, Kenichi; Tanaka, Hiroko; Hama, Asahito; Sanada, Masashi; Takahashi, Yoshiyuki; Kanno, Hitoshi; Yamaguchi, Hiroki; Ohga, Shouichi; Manabe, Atsushi; Harigae, Hideo; Kunishima, Shinji; Ishii, Eiichi; Kobayashi, Masao; Koike, Kenichi; Watanabe, Kenichiro; Ito, Etsuro; Takata, Minoru; Yabe, Miharu; Ogawa, Seishi; Miyano, Satoru; Kojima, Seiji.
Afiliación
  • Muramatsu H; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Okuno Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Yoshida K; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Shiraishi Y; Laboratory of DNA Information Analysis, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Doisaki S; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Narita A; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Sakaguchi H; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kawashima N; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Wang X; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Xu Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Chiba K; Laboratory of DNA Information Analysis, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Tanaka H; Laboratory of DNA Information Analysis, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Hama A; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Sanada M; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Takahashi Y; Department of Advanced Diagnosis, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Kanno H; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Yamaguchi H; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, Japan.
  • Ohga S; Department of Hematology, Nippon Medical School, Tokyo, Japan.
  • Manabe A; Department of Pediatrics, Yamaguchi University Graduate School of Medicine, Ube, Japan.
  • Harigae H; Department of Pediatrics, St. Luke's International Hospital, Tokyo, Japan.
  • Kunishima S; Department of Hematology and Rheumatology, Tohoku University Graduate School, Sendai, Japan.
  • Ishii E; Department of Advanced Diagnosis, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Kobayashi M; Department of Pediatrics, Ehime University Graduate School of Medicine, Ehime, Japan.
  • Koike K; Department of Pediatrics, Hiroshima University Hospital, Hiroshima, Japan.
  • Watanabe K; Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
  • Ito E; Department of Hematology/Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.
  • Takata M; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Yabe M; Laboratory of DNA Damage Signaling, Department of Late Effects Studies, Radiation Biology Center, Kyoto University, Kyoto, Japan.
  • Ogawa S; Department of Cell Transplantation and Regenerative Medicine, Tokai University Hospital, Isehara, Japan.
  • Miyano S; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Kojima S; Laboratory of DNA Information Analysis, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Genet Med ; 19(7): 796-802, 2017 07.
Article en En | MEDLINE | ID: mdl-28102861
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades de la Médula Ósea / Secuenciación de Nucleótidos de Alto Rendimiento / Hemoglobinuria Paroxística / Anemia Aplásica Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades de la Médula Ósea / Secuenciación de Nucleótidos de Alto Rendimiento / Hemoglobinuria Paroxística / Anemia Aplásica Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Japón