Liu WQ - Search Results

1

A Rare Case of Hb H Disease and Systemic Lupus Erythematosus.

Lin QY, Chen DY, Kong S, Liu WQ, Sun XF, Li DZ. Lin QY, et al. Among authors: liu wq. Hemoglobin. 2021 Jan;45(1):66-68. doi: 10.1080/03630269.2021.1886945. Epub 2021 Feb 16. Hemoglobin. 2021. PMID: 33593224

2

Skewed X chromosome inactivation in diploid and triploid female human embryonic stem cells.

Liu W, Sun X. Liu W, et al. Hum Reprod. 2009 Aug;24(8):1834-43. doi: 10.1093/humrep/dep126. Epub 2009 May 8. Hum Reprod. 2009. PMID: 19429659

3

Prenatal diagnosis of Roberts syndrome in a Chinese family based on ultrasound findings and whole exome sequencing: a case report.

Zhu L, Cao D, Chen M, Zhang H, Sun X, Liu W. Zhu L, et al. BMC Med Genomics. 2022 Jan 29;15(1):16. doi: 10.1186/s12920-022-01161-8. BMC Med Genomics. 2022. PMID: 35093090 Free PMC article.

4

Similar biological characteristics of human embryonic stem cell lines with normal and abnormal karyotypes.

Sun X, Long X, Yin Y, Jiang Y, Chen X, Liu W, Zhang W, Du H, Li S, Zheng Y, Kong S, Pang Q, Shi Y, Huang Y, Huang S, Liao B, Xiao G, Wang W. Sun X, et al. Hum Reprod. 2008 Oct;23(10):2185-93. doi: 10.1093/humrep/den137. Epub 2008 Jul 8. Hum Reprod. 2008. PMID: 18611919 Free PMC article.

5

Elevated hemoglobin A2 as a marker for β-thalassemia trait in pregnant women.

Ou Z, Li Q, Liu W, Sun X. Ou Z, et al. Tohoku J Exp Med. 2011 Mar;223(3):223-6. doi: 10.1620/tjem.223.223. Tohoku J Exp Med. 2011. PMID: 21403433 Free article.

6

[Clinical practice guidelines for the diagnosis of regions of homozygosity and uniparental disomy].

Zhu L, Zhang H, Li Z, Liu W, Sun X. Zhu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Nov 10;38(11):1140-1144. doi: 10.3760/cma.j.cn511374-20210303-00178. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34729761 Chinese.

7

[Clinical practice guidelines for the diagnosis of regions of homozygosity and uniparental disomy].

Zhu L, Zhang H, Li Z, Liu W, Sun X. Zhu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Nov 10;38(11):1140-1144. doi: 10.3760/cma.j.cn511374-20210303-00178. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34839523 Chinese.

8

[Comprehensive genetic analysis in first or second trimester pregnancy loss using chromosomal microarray with single nucleotide polymorphism probes].

Zhu L, Zhang H, Du Q, Sun X, Liu W. Zhu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jun 10;39(6):576-580. doi: 10.3760/cma.j.cn511374-20210506-00387. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35773758 Chinese.

9

Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations.

Liu W, Zhang H, Wang J, Yu G, Qiu W, Li Z, Chen M, Choy KW, Sun X. Liu W, et al. Mol Cytogenet. 2015 Nov 4;8:85. doi: 10.1186/s13039-015-0190-z. eCollection 2015. Mol Cytogenet. 2015. PMID: 26539248 Free PMC article.

10

Prenatal diagnosis of hemivertebrae--A likely association with 7q deletion.

Song YQ, Chen M, Yang ZL, He WY, Liu WQ, Li Y, Gong YF, Wang JY, Sun XF, Chen XJ. Song YQ, et al. Among authors: liu wq. Taiwan J Obstet Gynecol. 2016 Feb;55(1):112-6. doi: 10.1016/j.tjog.2015.05.004. Taiwan J Obstet Gynecol. 2016. PMID: 26927261 Free article. Review.

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