Kong S - Search Results

1

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. Among authors: kong s. 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.

2

[Cultivation and karyotype analysis of the human embryonic stem cells HUES4].

Zhang WH, Sun XF, Kong S, Jiang YH, Zheng YH, Yin YF. Zhang WH, et al. Among authors: kong s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Jun;24(3):275-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17557236 Chinese.

3

[The establishment and clinical application of multicolor fluorescence in situ hybridization].

Li Q, Sun XF, Chen XJ, Kong S, Zheng YH, Huang YY. Li Q, et al. Among authors: kong s. Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):45-7. Beijing Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 15719040 Free article. Chinese.

4

[Detect maternal serum fetal DNA for prenatal diagnosis].

Huang Y, Chen X, Kong S, Zheng Y, Zhou H. Huang Y, et al. Among authors: kong s. Zhonghua Fu Chan Ke Za Zhi. 2002 Dec;37(12):715-7. Zhonghua Fu Chan Ke Za Zhi. 2002. PMID: 12622911 Chinese.

5

Different culture method changing CD105 expression in amniotic fluid MSCs without affecting differentiation ability or immune function.

Wang D, Liu N, Xie Y, Song B, Kong S, Sun X. Wang D, et al. Among authors: kong s. J Cell Mol Med. 2020 Apr;24(7):4212-4222. doi: 10.1111/jcmm.15081. Epub 2020 Mar 2. J Cell Mol Med. 2020. PMID: 32119193 Free PMC article.

6

Cytogenic and molecular studies of male infertility in cases of Y chromosome balanced reciprocal translocation.

Wang D, Chen R, Kong S, Pan QY, Zheng YH, Qiu WJ, Fan Y, Sun XF. Wang D, et al. Among authors: kong s. Mol Med Rep. 2017 Aug;16(2):2051-2054. doi: 10.3892/mmr.2017.6835. Epub 2017 Jun 21. Mol Med Rep. 2017. PMID: 28656231

7

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: kong s. Hemoglobin. 2021 Jan;45(1):66-68. doi: 10.1080/03630269.2021.1886945. Epub 2021 Feb 16. Hemoglobin. 2021. PMID: 33593224

8

FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset.

Yuan H, Huang L, Hu X, Li Q, Sun X, Xie Y, Kong S, Wang X. Yuan H, et al. Among authors: kong s. Orphanet J Rare Dis. 2016 Jul 2;11(1):89. doi: 10.1186/s13023-016-0465-4. Orphanet J Rare Dis. 2016. PMID: 27370225 Free PMC article.

9

Psychomotor retardation with a 1q42.11-q42.12 deletion.

He J, Xie Y, Kong S, Qiu W, Wang X, Wang D, Sun X, Sun D. He J, et al. Among authors: kong s. Hereditas. 2017 Mar 6;154:6. doi: 10.1186/s41065-016-0022-0. eCollection 2017. Hereditas. 2017. PMID: 28286461 Free PMC article.

10

Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review.

Liang Y, Xie Y, Kong S, Pan Q, Qiu W, Wang D, Li M, Lin S, Liu Z, Sun X. Liang Y, et al. Among authors: kong s. Front Genet. 2022 Feb 24;13:792539. doi: 10.3389/fgene.2022.792539. eCollection 2022. Front Genet. 2022. PMID: 35281846 Free PMC article.

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