Liang Z - Search Results

1

A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.

Dong Z, Jiang L, Yang C, Hu H, Wang X, Chen H, Choy KW, Hu H, Dong Y, Hu B, Xu J, Long Y, Cao S, Chen H, Wang WJ, Jiang H, Xu F, Yao H, Xu X, Liang Z. Dong Z, et al. Among authors: liang z. Hum Mutat. 2014 May;35(5):625-36. doi: 10.1002/humu.22541. Epub 2014 Apr 9. Hum Mutat. 2014. PMID: 24610732

2

Deletion of a single-copy DAAM1 gene in congenital heart defect: a case report.

Bao B, Zhang L, Hu H, Yin S, Liang Z. Bao B, et al. Among authors: liang z. BMC Med Genet. 2012 Aug 2;13:63. doi: 10.1186/1471-2350-13-63. BMC Med Genet. 2012. PMID: 22857009 Free PMC article.

3

Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.

Yao H, Zhang L, Zhang H, Jiang F, Hu H, Chen F, Jiang H, Mu F, Zhao L, Liang Z, Wang W. Yao H, et al. Among authors: liang z. Prenat Diagn. 2012 Nov;32(11):1114-6. doi: 10.1002/pd.3946. Epub 2012 Aug 18. Prenat Diagn. 2012. PMID: 22903289 No abstract available.

4

Prenatal diagnosis of de novo partial trisomy 18p and partial monosomy 18q recurrent in a family with fatal aortic coarctation.

Hu H, Hao J, Yao H, Chang Q, Li R, Zhang X, Liang Z. Hu H, et al. Among authors: liang z. Gene. 2013 Mar 15;517(1):132-6. doi: 10.1016/j.gene.2012.12.001. Epub 2012 Dec 8. Gene. 2013. PMID: 23232358

5

Karyotypic and molecular genetic changes associated with fetal cardiovascular abnormalities: results of a retrospective 4-year ultrasonic diagnosis study.

Bao B, Wang Y, Hu H, Yao H, Li Y, Tang S, Zheng L, Xu Y, Liang Z. Bao B, et al. Among authors: liang z. Int J Biol Sci. 2013 May 9;9(5):463-71. doi: 10.7150/ijbs.5404. Print 2013. Int J Biol Sci. 2013. PMID: 23678296 Free PMC article.

6

Distinct karyotypes in two offspring of a man with jumping translocation karyotype 45,XY,der(16)t(16;22)(q24;q11.2), -22 [59]/45,XY,der(1)t(1;22)(p36;q11.2), -22 [11]/45,XY,der(22)t(22;22)(p13;q11.2), -22 [10].

Hu H, Yao H, Dong Y, Long Y, Xu L, Hu B, Xu G, Liang Z. Hu H, et al. Among authors: liang z. Am J Med Genet A. 2014 Aug;164A(8):2048-53. doi: 10.1002/ajmg.a.36560. Epub 2014 Apr 15. Am J Med Genet A. 2014. PMID: 24737738

7

Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.

Dong Y, Yi Y, Yao H, Yang Z, Hu H, Liu J, Gao C, Zhang M, Zhou L, Asan, Yi X, Liang Z. Dong Y, et al. Among authors: liang z. BMC Med Genet. 2016 Mar 15;17:23. doi: 10.1186/s12881-016-0286-2. BMC Med Genet. 2016. PMID: 26980296 Free PMC article.

8

Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women.

Yao H, Gao Y, Zhao J, Zhang R, Xu H, Hu H, Luo Y, Yuan Y, Fu M, Zhang H, Jiang H, Wang W, Yang H, Wang J, Liang Z, Chen F. Yao H, et al. Among authors: liang z. Sci China Life Sci. 2019 Feb;62(2):215-224. doi: 10.1007/s11427-017-9344-7. Epub 2018 Aug 2. Sci China Life Sci. 2019. PMID: 30076564

9

Comprehensive genomic variation profiling of cervical intraepithelial neoplasia and cervical cancer identifies potential targets for cervical cancer early warning.

Huang J, Qian Z, Gong Y, Wang Y, Guan Y, Han Y, Yi X, Huang W, Ji L, Xu J, Su M, Yuan Q, Cui S, Zhang J, Bao C, Liu W, Chen X, Zhang M, Gao X, Wu R, Zhang Y, Xu H, Zhu S, Zhu H, Yang L, Xu X, Zhou P, Liang Z. Huang J, et al. Among authors: liang z. J Med Genet. 2019 Mar;56(3):186-194. doi: 10.1136/jmedgenet-2018-105745. Epub 2018 Dec 19. J Med Genet. 2019. PMID: 30567904 Free PMC article.

10

Prenatal diagnosis of familial submicroscopic duplication at 18q22.3 without phenotypic abnormalities.

Hu H, Ma Y, Zhang R, Xu J, Hu B, Long Y, Xu L, Yao H, Liang Z. Hu H, et al. Among authors: liang z. Taiwan J Obstet Gynecol. 2020 May;59(3):446-450. doi: 10.1016/j.tjog.2020.03.021. Taiwan J Obstet Gynecol. 2020. PMID: 32416897 Free article.

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