Associated Papers
Exome sequencing for assessing the risk of 453 monogenic disorders in offspring: A study of 832 Chinese couples.
Ding X et al.
Clinical and Translational Medicine, 2024
39456122 (PubMed )
Supplement: CTM2-14-e70074-s003.xlsx › Table_S3
Early prenatal diagnosis of spondylocostal dysostosis caused by a novel variant in MESP2.
Zhou Y et al.
Congenital Anomalies, 2024
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