Li Y - Search Results

1

[Clinical features and genetics analysis of a Chinese pedigree affected with developmental and epileptic encephalopathy 9].

Zhi Y, Wang T, Zhang P, Sun Y, Li J, Li Y. Zhi Y, et al. Among authors: li y, li j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Sep 10;39(9):969-973. doi: 10.3760/cma.j.cn511374-20210819-00680. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36082567 Chinese.

2

[Karyotype analysis using cells cultured from fetal bladder centesis].

Gao J, Rong LM, Mei B, Yu XP, Guo WC, Li Y. Gao J, et al. Among authors: li y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Apr;30(2):207-9. doi: 10.3760/cma.j.issn.1003-9406.2013.04.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23568737 Chinese.

3

Polycystic Ovary Syndrome is Associated with Elevated Periostin Levels.

Chen X, Huo L, Ren L, Li Y, Sun Y, Li Y, Zhang P, Chen S, Song GY. Chen X, et al. Among authors: li y. Exp Clin Endocrinol Diabetes. 2019 Oct;127(9):571-577. doi: 10.1055/a-0752-0061. Epub 2018 Oct 29. Exp Clin Endocrinol Diabetes. 2019. PMID: 30372763 Clinical Trial.

4

[Correlation of thickened nuchal fold with fetal chromosomal abnormalities among 919 cases].

Ma L, Luo Y, Rong L, Huo P, Gao J, Li Y. Ma L, et al. Among authors: li y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):874-876. doi: 10.3760/cma.j.issn.1003-9406.2019.09.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515779 Chinese.

5

Cytogenetic analysis of 3387 umbilical cord blood in pregnant women at high risk for chromosomal abnormalities.

Sun Y, Zhang P, Zhang N, Rong L, Yu X, Huang X, Li Y. Sun Y, et al. Among authors: li y. Mol Cytogenet. 2020 Jan 23;13:2. doi: 10.1186/s13039-020-0469-6. eCollection 2020. Mol Cytogenet. 2020. PMID: 31998409 Free PMC article.

6

Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array.

Zhang P, Sun Y, Huo P, Tian H, Gao J, Li Y. Zhang P, et al. Among authors: li y. Mol Cytogenet. 2020 Apr 10;13:12. doi: 10.1186/s13039-020-00480-8. eCollection 2020. Mol Cytogenet. 2020. PMID: 32308739 Free PMC article.

7

Prenatal diagnosis and neonatal phenotype of a de novo microdeletion of 17p11.2p12 associated with Smith-Magenis syndrome and external genital defects.

Zhang P, Sun Y, Tian H, Rong L, Wang F, Yu X, Li Y, Gao J. Zhang P, et al. Among authors: li y. J Genet. 2020;99:50. J Genet. 2020. PMID: 32661203 Free article.

8

Prenatal diagnosis of the Dandy-Walker malformation associated with partial trisomy 12p and distal 15q deletion.

Sun Y, Zhang N, Tian H, Zhang P, Li Y. Sun Y, et al. Among authors: li y. J Genet. 2021;100:40. J Genet. 2021. PMID: 34238780 Free article.

9

A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly.

Wang T, Liu YX, Luo FM, Dong Y, Li YL, Fan LL. Wang T, et al. Among authors: li yl. Front Pediatr. 2021 Nov 29;9:774575. doi: 10.3389/fped.2021.774575. eCollection 2021. Front Pediatr. 2021. PMID: 34912761 Free PMC article.

10

A case of complex balanced chromosomal translocations associated with adverse pregnancy outcomes.

Luo Y, Lu H, Zhang Y, Cui Z, Zhang P, Li Y. Luo Y, et al. Among authors: li y. Mol Cytogenet. 2022 Aug 21;15(1):37. doi: 10.1186/s13039-022-00615-z. Mol Cytogenet. 2022. PMID: 35989338 Free PMC article.

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