Li Y - Search Results

1

Risk of birth defects in children conceived with assisted reproductive technology: A meta-analysis.

Lu Y, Liu L, Zhang P, Sun Y, Ma C, Li Y. Lu Y, et al. Among authors: li y. Medicine (Baltimore). 2022 Dec 30;101(52):e32405. doi: 10.1097/MD.0000000000032405. Medicine (Baltimore). 2022. PMID: 36596016 Free PMC article.

2

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.

3

Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.

Ma C, Liu L, Wang FN, Tian HS, Luo Y, Yu R, Fan LL, Li YL. Ma C, et al. Among authors: li yl. BMC Med Genet. 2019 Nov 6;20(1):169. doi: 10.1186/s12881-019-0917-5. BMC Med Genet. 2019. PMID: 31694554 Free PMC article.

4

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.

5

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.

6

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.

7

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.

8

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.

9

[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.

10

[Diagnosis of a patient with Spinocerebellar ataxia type 29 due to a novel variant of ITPR1 gene].

Zhi YN, Liu J, Zhen C, Li J, Wang F, Luo Y, Zhang P, Zhang M, Li Y. Zhi YN, et al. Among authors: li y, li j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Jan 10;40(1):76-80. doi: 10.3760/cma.j.cn511374-20220110-00022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36585006 Chinese.

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