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PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene.
Kato, Maki; Kato, Takema; Hosoba, Eriko; Ohashi, Masanao; Fujisaki, Midori; Ozaki, Mamoru; Yamaguchi, Masatoshi; Sameshima, Hiroshi; Kurahashi, Hiroki.
Affiliation
  • Kato M; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
  • Kato T; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
  • Hosoba E; Genome and Transcriptome Analysis Center, Fujita Health University, Toyoake, Japan.
  • Ohashi M; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
  • Fujisaki M; Department of Obstetrics and Gynecology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Ozaki M; Department of Obstetrics and Gynecology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Yamaguchi M; Department of Advanced Medicine, Division of Genomic Medicine, Medical Research Institute, Kanazawa Medical University, Ishikawa, Japan.
  • Sameshima H; Department of Obstetrics and Gynecology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Kurahashi H; Department of Obstetrics and Gynecology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Hum Genome Var ; 4: 17021, 2017.
Article in En | MEDLINE | ID: mdl-28611924
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Hum Genome Var Year: 2017 Type: Article Affiliation country: Japan
Fulltext
Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Hum Genome Var Year: 2017 Type: Article Affiliation country: Japan