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Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics.
Dong, Zirui; Wang, Huilin; Chen, Haixiao; Jiang, Hui; Yuan, Jianying; Yang, Zhenjun; Wang, Wen-Jing; Xu, Fengping; Guo, Xiaosen; Cao, Ye; Zhu, Zhenzhen; Geng, Chunyu; Cheung, Wan Chee; Kwok, Yvonne K; Yang, Huanming; Leung, Tak Yeung; Morton, Cynthia C; Cheung, Sau Wai; Choy, Kwong Wai.
Afiliación
  • Dong Z; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
  • Wang H; BGI-Shenzhen, Shenzhen, China.
  • Chen H; Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
  • Jiang H; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
  • Yuan J; Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
  • Yang Z; Department of Central Laboratory, Bao'an Maternity and Child Healthcare Hospital, Jinan University School of Medicine, Key Laboratory of Birth Defects Research, Birth Defects Prevention Research and Transformation Team, Shenzhen, China.
  • Wang WJ; BGI-Shenzhen, Shenzhen, China.
  • Xu F; China National Genebank-Shenzhen, BGI-Shenzhen, Shenzhen, China.
  • Guo X; BGI-Shenzhen, Shenzhen, China.
  • Cao Y; China National Genebank-Shenzhen, BGI-Shenzhen, Shenzhen, China.
  • Zhu Z; BGI-Shenzhen, Shenzhen, China.
  • Geng C; China National Genebank-Shenzhen, BGI-Shenzhen, Shenzhen, China.
  • Cheung WC; BGI-Shenzhen, Shenzhen, China.
  • Kwok YK; China National Genebank-Shenzhen, BGI-Shenzhen, Shenzhen, China.
  • Yang H; BGI-Shenzhen, Shenzhen, China.
  • Leung TY; China National Genebank-Shenzhen, BGI-Shenzhen, Shenzhen, China.
  • Morton CC; BGI-Shenzhen, Shenzhen, China.
  • Cheung SW; China National Genebank-Shenzhen, BGI-Shenzhen, Shenzhen, China.
  • Choy KW; Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Genet Med ; 20(7): 697-707, 2018 07.
Article en En | MEDLINE | ID: mdl-29095815
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Análisis Citogenético Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: China
Texto completo
Añadir a Mi BVS
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Análisis Citogenético Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: China