Wang W - Search Results

1

Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing.

Wang T, Duan C, Shen C, Xiang J, He Q, Ding J, Wen P, Zhang Q, Wang W, Liu M, Li H, Li H, Zhang L. Wang T, et al. Among authors: wang w. Mol Cytogenet. 2016 Jan 12;9:3. doi: 10.1186/s13039-016-0213-4. eCollection 2016. Mol Cytogenet. 2016. PMID: 26759606 Free PMC article.

2

[Identification of human small supernumerary marker chromosomes and discussion of its research value].

Ou J, Wang W, Duan CY, Fu WY, Liu YL, Sun J, Zhong HL, Li H. Ou J, et al. Among authors: wang w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):91-4. doi: 10.3760/cma.j.issn.1003-9406.2013.01.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450489 Chinese.

3

Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection.

Ou J, Wang W, Feng T, Liao L, Meng Q, Zou Q, Ding J, Zheng A, Duan C, Li P, Liu Q, Lin C, Li H. Ou J, et al. Among authors: wang w. Mol Cytogenet. 2015 Dec 30;8:105. doi: 10.1186/s13039-015-0207-7. eCollection 2015. Mol Cytogenet. 2015. PMID: 26719770 Free PMC article.

4

Characterization of three small supernumerary marker chromosomes (sSMC) in humans.

Ou J, Wang W, Liehr T, Klein E, Hamid AB, Wang F, Duan C, Li H. Ou J, et al. Among authors: wang w, wang f. J Matern Fetal Neonatal Med. 2013 Jan;26(1):106-8. doi: 10.3109/14767058.2012.732129. Epub 2012 Oct 11. J Matern Fetal Neonatal Med. 2013. PMID: 23013067 Free article.

5

[The value of blastocyst culture on preimplantation genetic diagnosis].

Ou J, Wang W, Ma Y, Zhou Z, Ding J, Wang F, Duan C, Li L, Zheng A, Chong W, Choy R, Li H. Ou J, et al. Among authors: wang w, wang f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Jun;32(3):312-7. doi: 10.3760/cma.j.issn.1003-9406.2015.03.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26037339 Chinese.

6

[Identification of de novo chromosomal structural abnormalities using whole genome sequencing].

Zhang Q, Ou J, Wang W, Feng T, Duan C, Li P, Lin C, Li H. Zhang Q, et al. Among authors: wang w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):96-99. doi: 10.3760/cma.j.issn.1003-9406.2018.01.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419871 Chinese.

7

[Prenatal diagnosis for two families of congenital factor V deficiency].

Cao LJ, Wang ZY, Li H, Wang W, Zhang W, Ding J, Yu ZQ, Bai X, Ruan CG. Cao LJ, et al. Among authors: wang w, wang zy. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):679-82. doi: 10.3760/cma.j.issn.1003-9406.2011.06.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161104 Chinese.

8

[Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].

Li H, Ding J, Wang W, Chen Y, Lu W, Shao H, Wu BL. Li H, et al. Among authors: wang w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):318-22. doi: 10.3760/cma.j.issn.1003-9406.2009.03.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19504448 Chinese.

9

SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.

Li H, Wang B, Liu D, Wang T, Li Q, Wang W, Li H. Li H, et al. Among authors: wang w, wang t, wang b. Genomics. 2015 Aug;106(2):83-7. doi: 10.1016/j.ygeno.2015.05.004. Epub 2015 May 22. Genomics. 2015. PMID: 26004784 Free article.

10

17β-Oestradiol promotes differentiation of human embryonic stem cells into dopamine neurons via cross-talk between insulin-like growth factors-1 and oestrogen receptor β.

Li H, Ding C, Ding ZL, Ling M, Wang T, Wang W, Huang B. Li H, et al. Among authors: wang w, wang t. J Cell Mol Med. 2017 Aug;21(8):1605-1618. doi: 10.1111/jcmm.13090. Epub 2017 Feb 28. J Cell Mol Med. 2017. PMID: 28244646 Free PMC article.

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