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MeSH:(Dual Oxidases/genetics*)

1.DUOX2 mutations in children with congenital hypothyroidism.

Jian CHAI ; Xiao-Long YANG ; Ming-Zhen GUO ; Lu LIU ; Shi-Guo LIU ; Sheng-Li YAN ; Yin-Lin GE

Chinese Journal of Contemporary Pediatrics 2015;17(1):40-44

2.Analysis of a child with Very early onset inflammatory bowel disease due to compound heterozygous variants of IL10RA and DUOX2 genes.

Cuifang ZHENG ; Wenhui HU ; Zhuowen YU ; Kuiran DONG ; Ying HUANG

Chinese Journal of Medical Genetics 2023;40(11):1404-1408

3.Results of neonatal screening for congenital hypothyroidism and hyperphenylalaninemia in Zhejiang province from 1999 to 2022.

Duo ZHOU ; Rulai YANG ; Xinwen HUANG ; Xiaolei HUANG ; Xin YANG ; Huaqing MAO ; Jianbin YANG ; Zhengyan ZHAO

Journal of Zhejiang University. Medical sciences 2023;52(6):683-692

4.Variant analysis of a patient with dyshormonogenesis due to congenital hypothyroidism.

Yuqiang LYU ; Ning XUE ; Kaihui ZHANG ; Junjie XU ; Yi LIU ; Zhongtao GAI

Chinese Journal of Medical Genetics 2018;35(6):836-839

5.Key Prediction Genes of Nasopharyngeal Carcinoma:Screening Based on Systematic Bioinformatics and Validation by Cell Experiments.

Zi-Kui HUANG ; Fei LI ; Yue-Zhou CHEN ; Jia-Ming LIU ; Jia-Jun LIU ; Su-Zhen LAN

Acta Academiae Medicinae Sinicae 2023;45(4):597-607

6.DUOX2 gene mutation in patients with congenital goiter with hypothyroidism.

Zhi-ping LÜ ; Gui-hua LI ; Wen-jie LI ; Shi-guo LIU

Chinese Journal of Pediatrics 2011;49(12):943-946

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