Huang C - Search Results

1

[Hybrid procedure for infants/children treatment with pulmonary stenosis under transesophageal echocardiographic guidance].

Xie L, Huang C, Wu S, Jin W, Gao L, Wu Q, Yang J, Wu Z, Zhao T, Yang Y, Song F. Xie L, et al. Among authors: huang c. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2016 Jul;41(7):691-5. doi: 10.11817/j.issn.1672-7347.2016.07.005. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2016. PMID: 27592572 Free article. Chinese.

2

Modified bjork procedure for tricuspid atresia with pulmonary hypertension.

Huang C, Gao L, Zhao T, Xu X, Yang Y. Huang C, et al. J Card Surg. 2011 Nov;26(6):657-9. doi: 10.1111/j.1540-8191.2011.01323.x. Epub 2011 Oct 5. J Card Surg. 2011. PMID: 21973011

3

Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies.

Chen JL, Yang YF, Huang C, Wang J, Yang JF, Tan ZP. Chen JL, et al. Among authors: huang c. Am J Med Genet A. 2012 Mar;158A(3):685-8. doi: 10.1002/ajmg.a.34434. Epub 2012 Feb 3. Am J Med Genet A. 2012. PMID: 22307725 No abstract available.

4

Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion.

Huang C, Yang YF, Yin N, Chen JL, Wang J, Zhang H, Tan ZP. Huang C, et al. Gene. 2012 May 1;498(2):308-10. doi: 10.1016/j.gene.2012.01.083. Epub 2012 Feb 16. Gene. 2012. PMID: 22366306

5

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome.

Luo C, Yang YF, Yin BL, Chen JL, Huang C, Zhang WZ, Wang J, Zhang H, Yang JF, Tan ZP. Luo C, et al. Among authors: huang c. Am J Med Genet A. 2012 Aug;158A(8):1918-23. doi: 10.1002/ajmg.a.35471. Epub 2012 Jul 11. Am J Med Genet A. 2012. PMID: 22786616

6

[Impact of Down syndrome on the surgical treatment of congenital heart defects].

Zhang W, Yang Y, Huang C, Zhao T. Zhang W, et al. Among authors: huang c. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2012 Jul;37(7):695-8. doi: 10.3969/j.issn.1672-7347.2012.07.008. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2012. PMID: 22886226 Chinese.

7

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Luo H, Xie L, Wang SZ, Chen JL, Huang C, Wang J, Yang JF, Zhang WZ, Yang YF, Tan ZP. Luo H, et al. Among authors: huang c. Eur J Med Genet. 2012 Nov;55(11):646-9. doi: 10.1016/j.ejmg.2012.07.006. Epub 2012 Jul 31. Eur J Med Genet. 2012. PMID: 22902603

8

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.

Yang YF, Ai Q, Huang C, Chen JL, Wang J, Xie L, Zhang WZ, Yang JF, Tan ZP. Yang YF, et al. Among authors: huang c. Gene. 2013 Oct 1;528(1):51-4. doi: 10.1016/j.gene.2013.03.145. Epub 2013 Apr 29. Gene. 2013. PMID: 23639964

9

Rare de novo copy number variants in patients with congenital pulmonary atresia.

Xie L, Chen JL, Zhang WZ, Wang SZ, Zhao TL, Huang C, Wang J, Yang JF, Yang YF, Tan ZP. Xie L, et al. Among authors: huang c. PLoS One. 2014 May 14;9(5):e96471. doi: 10.1371/journal.pone.0096471. eCollection 2014. PLoS One. 2014. PMID: 24826987 Free PMC article.

10

Echocardiographic assessment and guidance in minimally invasive surgical device closure of perimembranous ventricular septal defects.

Yang Y, Gao L, Xu X, Zhao T, Yang J, Gao Z, Yin N, Xiong L, Xie L, Huang C, Jin W, Wu Q. Yang Y, et al. Among authors: huang c. Heart Surg Forum. 2014 Aug;17(4):E206-11. doi: 10.1532/HSF98.2014340. Heart Surg Forum. 2014. PMID: 25179974 Clinical Trial.

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