Wei HW - Search Results

1

Malformations of cortical development: Fetal imaging and genetics.

Wang LL, Pan PS, Ma H, He C, Qin ZL, He W, Huang J, Tan SY, Meng DH, Wei HW, Yin AH. Wang LL, et al. Among authors: wei hw. Mol Genet Genomic Med. 2024 Apr;12(4):e2440. doi: 10.1002/mgg3.2440. Mol Genet Genomic Med. 2024. PMID: 38634212 Free PMC article.

2

Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.

Fu C, Wang J, Luo S, Yang Q, Li Q, Zheng H, Hu X, Su J, Zhang S, Chen R, Luo J, Zhang Y, Shen Y, Wei H, Meng D, Gui B, Zeng Z, Fan X, Chen S. Fu C, et al. Clin Chim Acta. 2016 Nov 1;462:127-132. doi: 10.1016/j.cca.2016.09.007. Epub 2016 Sep 13. Clin Chim Acta. 2016. PMID: 27637299

3

Monochorionic-Triamniotic Triplet Pregnancy Complicated by Twin Reversed Arterial Perfusion Sequence: Case Report and Literature Review.

Pan P, Luo G, Tang L, Rolle JD, Qin Y, Zeng Q, Wei J, Chen Y, Wei H. Pan P, et al. AJP Rep. 2017 Apr;7(2):e106-e110. doi: 10.1055/s-0037-1603917. Epub 2017 Jun 12. AJP Rep. 2017. PMID: 28611933 Free PMC article.

4

Etiology and Perinatal Outcome of Nonimmune Hydrops Fetalis in Southern China.

He S, Wang L, Pan P, Wei H, Meng D, Du J, Tian X, Zheng C, Qiu X, Luo G. He S, et al. AJP Rep. 2017 Apr;7(2):e111-e115. doi: 10.1055/s-0037-1603890. Epub 2017 Jun 12. AJP Rep. 2017. PMID: 28611934 Free PMC article.

5

Two novel pathogenic variants of L1CAM gene in two fetuses with isolated X‑linked hydrocephaly: A case report.

Xie B, Luo J, Lei Y, Yang Q, Li M, Yi S, Luo S, Wang J, Qin Z, Yang Z, Wei H, Fan X. Xie B, et al. Mol Med Rep. 2018 Dec;18(6):5760-5764. doi: 10.3892/mmr.2018.9583. Epub 2018 Oct 24. Mol Med Rep. 2018. PMID: 30365056

6

[Genetic testing and pregnancy outcome of 337 fetuses with urinary system anomalies].

Zeng S, Wang L, Luo S, Li Q, Qiu X, Gui C, Liu T, Wei H, Ma G, Fu C. Zeng S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Apr 10;36(4):306-309. doi: 10.3760/cma.j.issn.1003-9406.2019.04.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30950013 Chinese.

7

Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China.

Lai Y, Zhu X, He S, Dong Z, Tang Y, Xu F, Chen Y, Meng L, Tao Y, Yi S, Su J, Huang H, Luo J, Leung TY, Wei H. Lai Y, et al. Genes (Basel). 2021 Mar 25;12(4):478. doi: 10.3390/genes12040478. Genes (Basel). 2021. PMID: 33806256 Free PMC article.

8

The application of expanded noninvasive prenatal screening for genome-wide chromosomal abnormalities and genetic counseling.

Chen Y, Lai Y, Xu F, Qin H, Tang Y, Huang X, Meng L, Su J, Sun W, Shen Y, Wei H. Chen Y, et al. J Matern Fetal Neonatal Med. 2021 Aug;34(16):2710-2716. doi: 10.1080/14767058.2021.1907333. Epub 2021 May 2. J Matern Fetal Neonatal Med. 2021. PMID: 33938369 Free article.

9

Study on the correlation between the ultrasound phenotype and copy number variation of abnormal embryo in spontaneous abortion.

Tan S, Pan P, Yang Z, Su J, Wei H. Tan S, et al. J Obstet Gynaecol Res. 2021 Nov;47(11):3779-3788. doi: 10.1111/jog.14987. Epub 2021 Sep 27. J Obstet Gynaecol Res. 2021. PMID: 34571575 Free PMC article.

10

[Clinical analysis of monochorionic-diamniotic twins with genetic discordance].

Tang L, Pan P, Sun W, Qin J, Qin J, Qin Y, Huang P, Wei H. Tang L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 May 10;40(5):538-542. doi: 10.3760/cma.j.cn511374-20221228-00895. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37102285 Chinese.

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