Wei H - Search Results

1

[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. Among authors: wei h. 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.

2

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. Among authors: wei j, wei h. 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.

3

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. Among authors: wei h. 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.

4

[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. Among authors: wei h. 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.

5

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. Among authors: wei h. 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.

6

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. Among authors: wei h. 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.

7

Epidemiology of birth defects based on a birth defects surveillance system in southwestern China and the associated risk factors.

Peng Z, Wei J, Chen B, Huang X, Song P, Liang L, He J, Feng B, Que T, Qin J, Xie Y, Qiu X, Wei H, He S. Peng Z, et al. Among authors: wei j, wei h. Front Pediatr. 2023 Jul 21;11:1165477. doi: 10.3389/fped.2023.1165477. eCollection 2023. Front Pediatr. 2023. PMID: 37547102 Free PMC article.

8

Comprehensive application of multiple molecular diagnostic techniques in pre-implantation genetic testing for monogenic.

Huang P, Lan Y, Zhou H, Lin L, Shu J, Wang C, Zhao X, Liang L, He S, Mou J, Zhang X, Qiu Q, Wei H. Huang P, et al. Among authors: wei h. Mol Genet Genomic Med. 2024 Jan;12(1):e2293. doi: 10.1002/mgg3.2293. Epub 2023 Oct 12. Mol Genet Genomic Med. 2024. PMID: 37828787 Free PMC article.

9

Appropriate whole genome amplification and pathogenic loci detection can improve the accuracy of preimplantation genetic diagnosis for deletional α-thalassemia.

Lan Y, Zhou H, He S, Shu J, Liang L, Wei H, Luo J, Wang C, Zhao X, Qiu Q, Huang P. Lan Y, et al. Among authors: wei h. Front Endocrinol (Lausanne). 2024 Mar 8;14:1176063. doi: 10.3389/fendo.2023.1176063. eCollection 2023. Front Endocrinol (Lausanne). 2024. PMID: 38523870 Free PMC article.

10

Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study.

Wang L, Liang P, Pan P, Su J, Qin J, Chen Z, Huang D, Sun W, Song P, Wei H. Wang L, et al. Among authors: wei h. Eur J Obstet Gynecol Reprod Biol. 2024 Jun;297:91-95. doi: 10.1016/j.ejogrb.2024.04.002. Epub 2024 Apr 6. Eur J Obstet Gynecol Reprod Biol. 2024. PMID: 38603985 Free article.

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