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The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.
Kato, Takema; Inagaki, Hidehito; Miyai, Syunsuke; Suzuki, Fumihiko; Naru, Yuki; Shinkai, Yasuko; Kato, Asuka; Kanyama, Kazuo; Mizuno, Seiji; Muramatsu, Yukako; Yamamoto, Toshiyuki; Shinya, Mitsuhisa; Tazaki, Yukiko; Hiwatashi, Sayuri; Ikeda, Toshiro; Ozaki, Mamoru; Kurahashi, Hiroki.
Afiliación
  • Kato T; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Inagaki H; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Miyai S; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Suzuki F; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Naru Y; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Shinkai Y; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Kato A; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Kanyama K; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Mizuno S; Department of Clinical Genetics, Central Hospital, Aichi Developmental Disability Center, Kasugai, Kasugai, Japan.
  • Muramatsu Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Yamamoto T; Institute of Medical Genetics, Tokyo Women's Medical University, Shinjuku, Japan.
  • Shinya M; Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.
  • Tazaki Y; Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima, Japan.
  • Hiwatashi S; Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.
  • Ikeda T; Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima, Japan.
  • Ozaki M; Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.
  • Kurahashi H; Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima, Japan.
Hum Genet ; 139(11): 1417-1427, 2020 Nov.
Article en En | MEDLINE | ID: mdl-32488466
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cromosomas / Eliminación de Secuencia / Duplicación de Gen / Trastornos de los Cromosomas / Inversión Cromosómica Límite: Humans Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cromosomas / Eliminación de Secuencia / Duplicación de Gen / Trastornos de los Cromosomas / Inversión Cromosómica Límite: Humans Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: Japón