Fan X - Search Results

1

Mosaic UPD(7q)mat in a patient with silver Russell syndrome.

Su J, Wang J, Fan X, Fu C, Zhang S, Zhang Y, Qin Z, Li H, Luo J, Li C, Jiang T, Shen Y. Su J, et al. Among authors: fan x. Mol Cytogenet. 2017 Oct 17;10:36. doi: 10.1186/s13039-017-0337-1. eCollection 2017. Mol Cytogenet. 2017. PMID: 29075327 Free PMC article.

2

[Relationship between alanine aminotransferase and overweight or obesity in children].

Fan X, Chen SK, Tang Q, Luo JS, Feng Y. Fan X, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Dec;13(12):951-4. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 22172257 Free article. Chinese.

3

[Epidemiological study on the association between obesity with metabolic syndrome in obese children and adolescents of Nanning city, Guangxi].

Chen SK, Luo JS, Qin YF, Fan X, Tang Q, Feng Y. Chen SK, et al. Among authors: fan x. Zhonghua Liu Xing Bing Xue Za Zhi. 2011 Oct;32(10):969-72. Zhonghua Liu Xing Bing Xue Za Zhi. 2011. PMID: 22333076 Chinese.

4

[Pulmonary surfactant associated gene variants in mixed ethnic population of Han and Zhuang].

Chen YJ, Chen SK, DePass K, Wegner DJ, Hamvas A, Nong GM, Wang YZ, Fan X, Luo JS. Chen YJ, et al. Among authors: fan x. Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):843-6. Zhonghua Er Ke Za Zhi. 2012. PMID: 23302616 Chinese.

5

[Gene distribution characteristics of deletional α-thalassemia in Guangxi region].

Zhang Q, Fan X, He S, Fu C, Tang Y, Chen Q, Wei Y, Zheng C. Zhang Q, et al. Among authors: fan x. Zhonghua Xue Ye Xue Za Zhi. 2014 Oct;35(10):941-3. doi: 10.3760/cma.j.issn.0253-2727.2014.10.015. Zhonghua Xue Ye Xue Za Zhi. 2014. PMID: 25339335 Chinese.

6

[Prevalence of hypertension and relationship between hypertension and obesity in children and adolescents in Nanning of Guangxi Province].

Luo JS, Chen SK, Fan X, Tang Q, Feng Y. Luo JS, et al. Among authors: fan x. Zhongguo Dang Dai Er Ke Za Zhi. 2014 Oct;16(10):1040-4. Zhongguo Dang Dai Er Ke Za Zhi. 2014. PMID: 25344188 Free article. Chinese.

7

Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism.

Fu C, Chen S, Chen R, Fan X, Luo J, Li C, Qian J. Fu C, et al. Among authors: fan x. Arq Bras Endocrinol Metabol. 2014 Nov;58(8):828-32. doi: 10.1590/0004-2730000003436. Epub 2014 Nov 1. Arq Bras Endocrinol Metabol. 2014. PMID: 25465605

8

Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3).

Chen R, Li C, Xie B, Wang J, Fan X, Luo J, Hu X, Chen S, Shen Y. Chen R, et al. Among authors: fan x. Mol Cytogenet. 2014 Dec 24;7(1):101. doi: 10.1186/s13039-014-0101-8. eCollection 2014. Mol Cytogenet. 2014. PMID: 25648949 Free PMC article.

9

EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome.

Li C, Chen R, Fan X, Luo J, Qian J, Wang J, Xie B, Shen Y, Chen S. Li C, et al. Among authors: fan x. BMC Med Genet. 2015 Apr 11;16:23. doi: 10.1186/s12881-015-0165-2. BMC Med Genet. 2015. PMID: 25928000 Free PMC article.

10

Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.

Fu C, Zhang S, Su J, Luo S, Zheng H, Wang J, Qin H, Chen Y, Shen Y, Hu X, Fan X, Luo J, Xie B, Chen R, Chen S. Fu C, et al. Among authors: fan x. J Endocrinol Invest. 2015 Nov;38(11):1219-24. doi: 10.1007/s40618-015-0382-8. Epub 2015 Sep 9. J Endocrinol Invest. 2015. PMID: 26349762

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

15,856 results

Search Page

Filters