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Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations.
Ogura, Hiromi; Ohga, Shouichi; Aoki, Takako; Utsugisawa, Taiju; Takahashi, Hidehiro; Iwai, Asayuki; Watanabe, Kenichiro; Okuno, Yusuke; Yoshida, Kenichi; Ogawa, Seishi; Miyano, Satoru; Kojima, Seiji; Yamamoto, Toshiyuki; Yamamoto-Shimojima, Keiko; Kanno, Hitoshi.
Afiliación
  • Ogura H; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, Japan.
  • Ohga S; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Aoki T; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, Japan.
  • Utsugisawa T; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, Japan.
  • Takahashi H; Department of Neonatology, Musashino Red Cross Hospital, Tokyo, Japan.
  • Iwai A; Department of Pediatrics, Shikoku Central Hospital, Ehime, Japan.
  • Watanabe K; Department of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.
  • Okuno Y; Center of Advanced Medicine and Clinical Research, Nagoya University, Aichi, Japan.
  • Yoshida K; Department of Pathology and Tumor Biology, Kyoto University Graduate School of Medicine Faculty of Medicine, Kyoto, Japan.
  • Ogawa S; Department of Pathology and Tumor Biology, Kyoto University Graduate School of Medicine Faculty of Medicine, Kyoto, Japan.
  • Miyano S; Institute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto, Japan.
  • Kojima S; Department of Medicine, Center for Hematology and Regenerative Medicine, Karolinska Institute, Stockholm, Sweden.
  • Yamamoto T; M&D Data Science Center, Tokyo Medical and Dental University, Tokyo, Japan.
  • Yamamoto-Shimojima K; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kanno H; Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.
Hum Genome Var ; 7(1): 42, 2020 Nov 27.
Article en En | MEDLINE | ID: mdl-33298904
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Hum Genome Var Año: 2020 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Hum Genome Var Año: 2020 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido