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Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing.
Yu, Dongyi; Zhang, Kai; Han, Meiyan; Pan, Wei; Chen, Ying; Wang, Yunfeng; Jiao, Hongyan; Duan, Ling; Zhu, Qiying; Song, Xiaojie; Hong, Yan; Chen, Chen; Wang, Juan; Hui, Feng; Huang, Linzhou; Chen, Chongjian; Du, Yang.
Afiliação
  • Yu D; Genetic Testing Center, Qingdao Women & Children Hospital, Qingdao University, Qingdao, China.
  • Zhang K; Genetic Testing Center, Qingdao Women & Children Hospital, Qingdao University, Qingdao, China.
  • Han M; Genetic Testing Center, Qingdao Women & Children Hospital, Qingdao University, Qingdao, China.
  • Pan W; The Center of Prenatal Diagnosis, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
  • Chen Y; Central Lab, Wuxi Maternity and Child Health Care Hospital, Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University, Wuxi, Jiangsu, China.
  • Wang Y; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Jiao H; The Branch Center of Prenatal Diagnosis, Hebei Maternity and Child Healthcare Hospital, Shijiazhuang, China.
  • Duan L; Department of Obstetrics, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Zhu Q; Department of Obstetrics, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Song X; Department of Obstetrics and Gynecology, Wuhan Women and Child Care Service Hospital, Wuhan, China.
  • Hong Y; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Chen C; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Wang J; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Hui F; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Huang L; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Chen C; Annoroad Gene Technology Co., Ltd, Beijing, China.
  • Du Y; Annoroad Gene Technology Co., Ltd, Beijing, China.
Mol Genet Genomic Med ; 7(6): e674, 2019 06.
Article em En | MEDLINE | ID: mdl-31004415
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos / Variações do Número de Cópias de DNA / Sequenciamento Completo do Genoma / Teste Pré-Natal não Invasivo / Aneuploidia Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos / Variações do Número de Cópias de DNA / Sequenciamento Completo do Genoma / Teste Pré-Natal não Invasivo / Aneuploidia Idioma: En Ano de publicação: 2019 Tipo de documento: Article