首页> Prenatal diagnosis> Low-Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses.

Low-Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses.

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第一作者： Lijuan,Pan

第一单位： Department of Obstetrics, Xiangya Hospital, Central South University, Changsha, China.

作者： Lijuan,Pan ^[1] ; Jiayu,Wu ^[2] ; Yi,Zhang ^[3] ; Desheng,Liang ^[2] ; Jing,Yuan ^[4] ; Jue,Wang ^[5] ; Yinchen,Shen ^[6] ; Junjie,Lu ^[7] ; Aihua,Xia ^[8] ; Zhenhui,Zhang ^[9] ; Jinchen,Li ^[3] ; Zhuo,Li ^[2] ; Lingqian,Wu ^[2]

作者单位： Department of Obstetrics, Xiangya Hospital, Central South University, Changsha, China. ^[1] Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, China. ^[2] Bioinformatics Center & National Clinical Research Centre for Geriatric Disorders & Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, China. ^[3] Department of Obstetrics and Gynecology, Prenatal Diagnosis Center, the First Affiliated Hospital of Anhui Medical University, Hefei, China. ^[4] Department of Obstetrics, the First Affiliated Hospital With Nanjing Medical University, Nanjing, China. ^[5] Department of Maternity Care, Nanning Maternity and Child Health Hospital, Nanning, China. ^[6] Department of Obstetrics and Gynecology, the Second Affiliated Hospital, Army Military Medical University, Chongqing, China. ^[7] Department of Obstetrics, Beihai People's Hospital, Beihai, China. ^[8] Department of Obstetrics, The Affiliated Changsha Hospital of Xiangya School of Medicine, Central South University (The First Hospital of Changsha), Changsha, China. ^[9]

关键词 aneuploidies low‐pass genome sequencing pathogenic/likely pathogenic copy number variations prenatal diagnosis ultrasonographic anomaly

DOI 10.1002/pd.70114

PMID 41793061

发布时间 2026-03-07

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