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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References

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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.