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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 10, 2023. (Total: 217827Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Thyroid Neoplasms and GNAS[original query]
Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer.
Scientific reports 2015 5 16129.
Yu Yang, Dong Li, Li Dapeng, Chuai Shaokun, Wu Zhigang, Zheng Xiangqian, Cheng Yanan, Han Lei, Yu Jinpu, Gao Mi
Inherited variants in genes somatically mutated in thyroid cancer.
PloS one 2017 12 (4): e0174995.
Campo Chiara, Köhler Aleksandra, Figlioli Gisella, Elisei Rossella, Romei Cristina, Cipollini Monica, Bambi Franco, Hemminki Kari, Gemignani Federica, Landi Stefano, Försti As
Increased Prevalence of Malignancies in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS): Data from a National Referral Center and the Dutch National Pathology Registry (PALGA).
Calcified tissue international 2020 Nov .
Hagelstein-Rotman M, Meier M E, Majoor B C J, Cleven A H G, Dijkstra P D S, Hamdy N A T, van de Sande M A J, Dekkers O M, Appelman-Dijkstra N
Cathepsin F genetic mutation is associated with familial papillary thyroid cancer.
The American journal of the medical sciences 2022 4 364 (4): 414-424.
Wang Yaqiong, Mei Jingzhao, Zhang Yujie, He Xianghui, Zheng Xiangqian, Tan Jian, Jia Qiang, Li Ning, Li Dihua, Wang Yan, Meng Zhaow
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