Xu Z - Search Results

1

Subgroup analysis of imaging scans, invasive examinations and prognosis in mild-to-moderate isolated foetal cerebral ventriculomegaly: a retrospective study in China.

Yang C, Chi X, Wang Y, Zhang C, Zhou R, Jia X, Qiao F, Xu Z. Yang C, et al. Among authors: xu z. J Int Med Res. 2024 Dec;52(12):3000605241301879. doi: 10.1177/03000605241301879. J Int Med Res. 2024. PMID: 39648848 Free PMC article.

2

Reproductive outcomes in couples with sporadic miscarriage after embryonic chromosomal microarray analysis.

Xia Z, Zhou R, Li Y, Meng L, Huang M, Tan J, Qiao F, Zhu H, Hu P, Zhu Q, Xu Z, Wang Y. Xia Z, et al. Among authors: xu z. Ann Med. 2023 Dec;55(1):837-848. doi: 10.1080/07853890.2023.2183986. Ann Med. 2023. PMID: 36869707 Free PMC article.

3

Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosis.

Hu P, Zhang Q, Cheng Q, Luo C, Zhang C, Zhou R, Meng L, Huang M, Wang Y, Wang Y, Qiao F, Xu Z. Hu P, et al. Among authors: xu z. Am J Obstet Gynecol. 2023 Sep;229(3):302.e1-302.e18. doi: 10.1016/j.ajog.2023.03.005. Epub 2023 Mar 11. Am J Obstet Gynecol. 2023. PMID: 36907537

4

Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis.

Zhang Q, Wang Y, Xu Y, Zhou R, Huang M, Qiao F, Meng L, Liu A, Zhou J, Li L, Ji X, Xu Z, Hu P. Zhang Q, et al. Among authors: xu y, xu z. Acta Obstet Gynecol Scand. 2023 Aug;102(8):1053-1062. doi: 10.1111/aogs.14613. Epub 2023 Jun 27. Acta Obstet Gynecol Scand. 2023. PMID: 37366235 Free PMC article.

5

Residual risk of clinically significant copy number variations in fetuses with nasal bone absence or hypoplasia after excluding non-invasive prenatal screening-detectable findings.

Xia Z, Zhou R, Xu Y, Li Y, Tan J, Luo C, Meng L, Huang M, Qiao F, Hu P, Mao P, Wu Y, Xu Z, Wang Y. Xia Z, et al. Among authors: xu y, xu z. Clin Chim Acta. 2024 Jan 15;553:117744. doi: 10.1016/j.cca.2023.117744. Epub 2023 Dec 27. Clin Chim Acta. 2024. PMID: 38158003

6

Prenatal diagnosis of chromosomal abnormalities using optical genome mapping vs chromosomal microarray.

Hu P, Xu Y, Zhang Q, Zhou R, Ji X, Wang Y, Xu Z. Hu P, et al. Among authors: xu y, xu z. Am J Obstet Gynecol. 2024 May;230(5):e82-e83. doi: 10.1016/j.ajog.2023.12.012. Epub 2023 Dec 13. Am J Obstet Gynecol. 2024. PMID: 38097028 No abstract available.

7

Reproductive outcomes in couples with recurrent pregnancy loss after embryonic chromosomal microarray analysis.

Li Y, Zhou R, Xia Z, Meng L, Huang M, Hu P, Xu Z, Wang Y. Li Y, et al. Among authors: xu z. J Assist Reprod Genet. 2024 Jan;41(1):161-170. doi: 10.1007/s10815-023-02971-0. Epub 2023 Oct 24. J Assist Reprod Genet. 2024. PMID: 37874532

8

Systematic analysis of copy number variants of uncertain significance partially overlapping with the haploinsufficient or triplosensitive genes in clinical testing.

Zhou R, Jiao J, Wang Y, Meng L, Li Y, Xu Y, Hu P, Xu Z. Zhou R, et al. Among authors: xu y, xu z. Ann Med. 2023;55(2):2276824. doi: 10.1080/07853890.2023.2276824. Epub 2023 Nov 2. Ann Med. 2023. PMID: 37917952 Free PMC article.

9

Comprehensive genetic analysis of facioscapulohumeral muscular dystrophy by Nanopore long-read whole-genome sequencing.

Huang M, Zhang Q, Jiao J, Shi J, Xu Y, Zhang C, Zhou R, Liu W, Liang Y, Chen H, Wang Y, Xu Z, Hu P. Huang M, et al. Among authors: xu y, xu z. J Transl Med. 2024 May 13;22(1):451. doi: 10.1186/s12967-024-05259-8. J Transl Med. 2024. PMID: 38741136 Free PMC article.

10

A Novel Splice Site Mutation in the FBN2 Gene in a Chinese Family with Congenital Contractural Arachnodactyly.

Zhang C, Qiao F, Cheng Q, Luo C, Zhang Q, Hu P, Xu Z. Zhang C, et al. Among authors: xu z. Biochem Genet. 2024 Aug;62(4):2495-2503. doi: 10.1007/s10528-023-10550-2. Epub 2023 Nov 14. Biochem Genet. 2024. PMID: 37962692 Free PMC article.

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