Exome sequencing for assessing the risk of 453 monogenic disorders in offspring: A study of 832 Chinese couples

Xulong Ding; Miao Jiang; Qin Hu; Ruiqing Tong; Lin Wang; Jinxing Lv; Ling Pan; Jianquan Hou; Jun He; Peng Zhou

doi:10.1002/ctm2.70074

Clinical and Translational Medicine ›› 2024, Vol. 14 ›› Issue (11) : e70074 DOI: 10.1002/ctm2.70074

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Exome sequencing for assessing the risk of 453 monogenic disorders in offspring: A study of 832 Chinese couples

Xulong Ding ¹^,^†
, Miao Jiang ²
, Qin Hu ³
, Ruiqing Tong ⁴
, Lin Wang ¹
, Jinxing Lv ⁴
, Ling Pan ³
, Jianquan Hou ⁵
, Jun He ¹^,⁶^,^†
, Peng Zhou ¹^,^†

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Xulong Ding,Miao Jiang,Qin Hu,Ruiqing Tong,Lin Wang,Jinxing Lv,Ling Pan,Jianquan Hou,Jun He,Peng Zhou. Exome sequencing for assessing the risk of 453 monogenic disorders in offspring: A study of 832 Chinese couples. Clinical and Translational Medicine, 2024, 14(11): e70074 DOI:10.1002/ctm2.70074

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2024 The Author(s). Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.