Lv W - Search Results

1

Noninvasive prenatal diagnosis for pregnancies at risk for β-thalassaemia: a retrospective study.

Lv W, Linpeng S, Li Z, Liang D, Jia Z, Meng D, Cram DS, Zhu H, Teng Y, Yin A, Wu L. Lv W, et al. BJOG. 2021 Jan;128(2):448-457. doi: 10.1111/1471-0528.16295. Epub 2020 May 28. BJOG. 2021. PMID: 32363759

2

A patient with apparently reciprocal translocation and cryptic 10p deletion.

Wu L, Liao X, Wang H, Zhou Z, Lv W, Liang D. Wu L, et al. Among authors: lv w. Am J Med Genet A. 2011 Jul;155A(7):1753-5. doi: 10.1002/ajmg.a.33734. Epub 2011 May 27. Am J Med Genet A. 2011. PMID: 21626668 No abstract available.

3

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.

Liang D, Lv W, Wang H, Xu L, Liu J, Li H, Hu L, Peng Y, Wu L. Liang D, et al. Among authors: lv w. Prenat Diagn. 2013 May;33(5):409-15. doi: 10.1002/pd.4033. Epub 2013 Jan 9. Prenat Diagn. 2013. PMID: 23299662

4

An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic mother.

Wu L, Liu J, Lv W, Wen J, Xia Y, Liang D. Wu L, et al. Among authors: lv w. Birth Defects Res A Clin Mol Teratol. 2013 Jul;97(7):467-70. doi: 10.1002/bdra.23118. Epub 2013 Jul 4. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 23828844

5

Phenotypic expansion of the interstitial 16p13.3 duplication: a case report and review of the literature.

Li Z, Liu J, Li H, Peng Y, Lv W, Long Z, Liang D, Wu L. Li Z, et al. Among authors: lv w. Gene. 2013 Dec 1;531(2):502-5. doi: 10.1016/j.gene.2013.09.006. Epub 2013 Sep 12. Gene. 2013. PMID: 24035902 Review.

6

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.

Liang D, Peng Y, Lv W, Deng L, Zhang Y, Li H, Yang P, Zhang J, Song Z, Xu G, Cram DS, Wu L. Liang D, et al. Among authors: lv w. J Mol Diagn. 2014 Sep;16(5):519-526. doi: 10.1016/j.jmoldx.2014.05.002. Epub 2014 Jul 3. J Mol Diagn. 2014. PMID: 24998187 Free article.

7

Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART).

Lv W, Wei X, Guo R, Liu Q, Zheng Y, Chang J, Bai T, Li H, Zhang J, Song Z, Cram DS, Liang D, Wu L. Lv W, et al. Clin Chem. 2015 Jan;61(1):172-81. doi: 10.1373/clinchem.2014.229328. Epub 2014 Nov 6. Clin Chem. 2015. PMID: 25376582

8

Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis.

Zhang S, Qin H, Lv W, Luo S, Wang J, Fu C, Ma R, Shen Y, Chen S, Wu L. Zhang S, et al. Among authors: lv w. Gene. 2016 Feb 15;577(2):187-92. doi: 10.1016/j.gene.2015.11.034. Epub 2015 Nov 25. Gene. 2016. PMID: 26625971

9

Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIII.

Huang Y, Mei L, Lv W, Li H, Zhang R, Pan Q, Tan H, Guo J, Luo X, Chen C, Liang D, Wu L. Huang Y, et al. Among authors: lv w. Clin Chim Acta. 2017 Jan;464:170-175. doi: 10.1016/j.cca.2016.11.019. Epub 2016 Nov 15. Clin Chim Acta. 2017. PMID: 27864101

10

Identification of a novel MIP frameshift mutation associated with congenital cataract in a Chinese family by whole-exome sequencing and functional analysis.

Long X, Huang Y, Tan H, Li Z, Zhang R, Linpeng S, Lv W, Cao Y, Li H, Liang D, Wu L. Long X, et al. Among authors: lv w. Eye (Lond). 2018 Aug;32(8):1359-1364. doi: 10.1038/s41433-018-0084-5. Epub 2018 Apr 26. Eye (Lond). 2018. PMID: 29695758 Free PMC article.

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