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[A consensus recommendation for the interpretation and reporting of exome sequencing in prenatal genetic diagnosis].
Genetic Disease Society Guangdong Precision Medicine Application Association Prenatal Diagnosis Group Maternal And Child Health Care Society Guangdong Medical Association Expert Committee Of Prenatal Diagnosis, Zhang Y, Liu W, Zhang J, Lin S, Huang H, Zhang WV, Ren Z, Wang Y, Yang Y, Yin A. Genetic Disease Society Guangdong Precision Medicine Application Association Prenatal Diagnosis Group Maternal And Child Health Care Society Guangdong Medical Association Expert Committee Of Prenatal Diagnosis, et al. Among authors: zhang wv, zhang j, zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Nov 10;37(11):1205-1212. doi: 10.3760/cma.j.cn511374-20200809-00593. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33179222 Chinese.
[Consensus on technological standards for non-invasive prenatal screening of pathogenic copy number variations by high-throughput sequencing of maternal plasma cell-free DNA].
Liu W, Yang J, Zhang J, Lu J, Chen Y, Zhu H, Xiang J, Wang Y, Wang M, Wang J, Wu Q, Yin A. Liu W, et al. Among authors: zhang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jul 10;38(7):613-619. doi: 10.3760/cma.j.cn511374-20201208-00855. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34247362 Chinese.
Placental methylation markers in normal and trisomy 21 tissues.
Yin YZ, She Q, Zhang J, Zhang PZ, Zhang Y, Lin JW, Ye YC. Yin YZ, et al. Among authors: zhang pz, zhang j, zhang y. Prenat Diagn. 2014 Jan;34(1):63-70. doi: 10.1002/pd.4256. Epub 2013 Nov 15. Prenat Diagn. 2014. PMID: 24166080
[Association of MDR1 gene polymorphisms with refractory epilepsy in children].
Gao L, Yin X, Li Y, Xiao H, Yang L, Fan H, Qi H, Zhang J, Feng J, Zheng F. Gao L, et al. Among authors: zhang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1073-1076. doi: 10.3760/cma.j.issn.1003-9406.2019.11.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703128 Chinese.
179,008 results
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