Fu C - Search Results

1

A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features.

Xie B, Fan X, Lei Y, Chen R, Wang J, Fu C, Yi S, Luo J, Zhang S, Yang Q, Chen S, Shen Y. Xie B, et al. Among authors: fu c. Mol Cytogenet. 2016 May 31;9:41. doi: 10.1186/s13039-016-0251-y. eCollection 2016. Mol Cytogenet. 2016. PMID: 27247625 Free PMC article.

2

[Genotypes of 1 571 cases of Hb H disease in Guangxi area].

Fu C, Chen S, Zhang Q, He S, Wei Y, Chen Q, Tang Y, Zheng C. Fu C, et al. Zhonghua Xue Ye Xue Za Zhi. 2014 Aug;35(8):728-31. doi: 10.3760/cma.j.issn.0253-2727.2014.08.013. Zhonghua Xue Ye Xue Za Zhi. 2014. PMID: 25152122 Chinese.

3

[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: fu c. 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.

4

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. 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

5

PAX8 pathogenic variants in Chinese patients with congenital hypothyroidism.

Fu C, Chen R, Zhang S, Luo S, Wang J, Chen Y, Zheng H, Su J, Hu X, Fan X, Luo J, Yi S, Lai Y, Li C, Xie B, Shen Y, Gu X, Chen S. Fu C, et al. Clin Chim Acta. 2015 Oct 23;450:322-6. doi: 10.1016/j.cca.2015.09.008. Epub 2015 Sep 8. Clin Chim Acta. 2015. PMID: 26362610

6

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: fu c. Gene. 2016 Feb 15;577(2):187-92. doi: 10.1016/j.gene.2015.11.034. Epub 2015 Nov 25. Gene. 2016. PMID: 26625971

7

Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism.

Hu X, Chen R, Fu C, Fan X, Wang J, Qian J, Yi S, Li C, Luo J, Su J, Zhang S, Xie B, Zheng H, Lai Y, Chen Y, Li H, Gu X, Chen S, Shen Y. Hu X, et al. Among authors: fu c. Mol Cell Endocrinol. 2016 Mar 5;423:60-6. doi: 10.1016/j.mce.2016.01.007. Epub 2016 Jan 8. Mol Cell Endocrinol. 2016. PMID: 26777470

8

Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism.

Fu C, Zheng H, Zhang S, Chen Y, Su J, Wang J, Xie B, Hu X, Fan X, Luo J, Li C, Chen R, Shen Y, Chen S. Fu C, et al. Arch Endocrinol Metab. 2016 Aug;60(4):323-7. doi: 10.1590/2359-3997000000108. Epub 2016 Feb 16. Arch Endocrinol Metab. 2016. PMID: 26886089 Free PMC article.

9

Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.

Fu C, Luo S, Zhang S, Wang J, Zheng H, Yang Q, Xie B, Hu X, Fan X, Luo J, Chen R, Su J, Shen Y, Gu X, Chen S. Fu C, et al. Clin Chim Acta. 2016 Jul 1;458:30-4. doi: 10.1016/j.cca.2016.04.019. Epub 2016 Apr 21. Clin Chim Acta. 2016. PMID: 27108200

10

de novo interstitial deletions at the 11q23.3-q24.2 region.

Su J, Chen R, Luo J, Fan X, Fu C, Wang J, He S, Hu X, Zhang S, Yi S, Chen S, Shen Y. Su J, et al. Among authors: fu c. Mol Cytogenet. 2016 May 5;9:39. doi: 10.1186/s13039-016-0247-7. eCollection 2016. Mol Cytogenet. 2016. PMID: 27158264 Free PMC article.

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