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[Clinical practice guidelines for Noonan syndrome].
Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Li X, Wang X, Wang J, Fu L, Luo X, Fu J, Shen Y. Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, et al. Among authors: wang x, wang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Mar 10;37(3):324-328. doi: 10.3760/cma.j.issn.1003-9406.2020.03.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32128752 Chinese.
A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal.
Wang J, Yu T, Wang Z, Ohte S, Yao RE, Zheng Z, Geng J, Cai H, Ge Y, Li Y, Xu Y, Zhang Q, Gusella JF, Fu Q, Pregizer S, Rosen V, Shen Y. Wang J, et al. Among authors: wang z. J Bone Miner Res. 2016 Apr;31(4):882-9. doi: 10.1002/jbmr.2761. Epub 2015 Dec 28. J Bone Miner Res. 2016. PMID: 26643732 Free PMC article.
Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience.
Hu X, Li N, Xu Y, Li G, Yu T, Yao RE, Fu L, Wang J, Yin L, Yin Y, Wang Y, Jin X, Wang X, Wang J, Shen Y. Hu X, et al. Among authors: wang x, wang j, wang y. Genet Med. 2018 Sep;20(9):1045-1053. doi: 10.1038/gim.2017.195. Epub 2017 Nov 2. Genet Med. 2018. PMID: 29095814 Free article.
[Genetic analysis of two children patients affected with CHARGE syndrome].
Li G, Li N, Xu Y, Li J, Ding Y, Shen Y, Wang X, Wang J. Li G, et al. Among authors: wang x, wang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):244-247. doi: 10.3760/cma.j.issn.1003-9406.2018.02.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29653002 Chinese.
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