HuGE Literature Finder
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Records 1-2
Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis.
Journal of clinical research in pediatric endocrinology 2015 Dec . Shiguo Liu, Jian Chai, Guohua Zheng, Huichao Li, Deguo |
Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.
BMC medical genetics 2010 11 (1): 81. Han Xueyao, Luo Yingying, Ren Qian, Zhang Xiuying, Wang Fang, Sun Xiuqin, Zhou Xianghai, Ji Lino |
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