Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing

Molecular Genetics & Genomic Medicine

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[1] Annoroad Gene Technology Co., Ltd, Beijing, China;Central Lab, Wuxi Maternity and Child Health Care Hospital, Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University, Wuxi, Jiangsu, China;Department of Obstetrics and Gynecology, Wuhan Women and Child Care Service Hospital, Wuhan, China;Department of Obstetrics, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China;Genetic Testing Center, Qingdao Women & Children Hospital, Qingdao University, Qingdao, China;The Branch Center of Prenatal Diagnosis, Hebei Maternity and Child Healthcare Hospital, Shijiazhuang, China;The Center of Prenatal Diagnosis, Affiliated Hospital of Guizhou Medical University, Guiyang, China;

关键词: cell‐free DNA;    chromosome aneuploidy;    NIPSCCD;    NIPT;    subchromosomal CNVs;   

DOI  :  10.1002/mgg3.674

来源: publisher

【 授权许可】

Unknown