Detalhe da pesquisa
1.
Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.
J Cell Mol Med;
22(4): 2190-2199, 2018 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29377512
2.
Association between DSCAM polymorphisms and non-syndromic Hirschsprung disease in Chinese population.
BMC Med Genet;
19(1): 116, 2018 07 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30005639
3.
Association of polymorphism in the VEGFA gene 3'-UTR +936T/C with susceptibility to biliary atresia in a Southern Chinese Han population.
J Clin Lab Anal;
32(4): e22342, 2018 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29251369
4.
Anti-proliferative effect of the extract of Guangzao (Fructus Choerospondiatis) on cultured rat cardiac fibroblasts.
J Tradit Chin Med;
35(6): 685-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26742315
5.
PDGFA gene rs9690350 polymorphism increases biliary atresia risk in Chinese children.
Biosci Rep;
40(7)2020 07 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32662506
6.
Establishment of an induced pluripotent stem cell model of Hirschsrpung disease, a congenital condition of the enteric nervous system, from a patient carrying a novel RET mutation.
Neuroreport;
29(12): 975-980, 2018 08 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29965875
7.
Association between NEFL Gene Polymorphisms and Neuroblastoma Risk in Chinese Children: A Two-Center Case-Control Study.
J Cancer;
9(3): 535-539, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29483959
8.
Bowel management program for pediatric postoperative fecal incontinence in China: A surgeon's experience.
Medicine (Baltimore);
96(22): e7078, 2017 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28562577
9.
Genetic and Clinical Analyses of Southern Chinese Children with Peutz-Jeghers Syndrome.
Genet Test Mol Biomarkers;
19(9): 528-31, 2015 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26225618
10.
[Surgical management of pyloric stenosis induced by gastrointestinal chemical burn in children].
Zhonghua Wei Chang Wai Ke Za Zhi;
16(5): 467-70, 2013 May.
Artigo
em Zh
| MEDLINE
| ID: mdl-23696406
11.
RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.
PLoS One;
6(12): e28986, 2011.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22174939