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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Hypogonadism and CCDC141[original query]
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism.
Clinical genetics 2019 Feb 95 (2): 320-324.
Kotan Leman D, Isik Emregul, Turan Ihsan, Mengen Eda, Akkus Gamze, Tastan Mehmet, Gurbuz Fatih, Yuksel Bilgin, Topaloglu A Kem
Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.
European journal of endocrinology 2020 6 183 (3): 245-254.
Hou Qiao, Wu Jiayu, Zhao Yaguang, Wang Xinying, Jiang Fang, Chen Dan-Na, Zheng Ruizhi, Men Meichao, Li Jia-
Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism.
Asian journal of andrology 2020 11 23 (3): 288-293.
Zhang Jian, Tang Shu-Yan, Zhu Xiao-Bin, Li Peng, Lu Jian-Qi, Cong Jiang-Shan, Wang Ling-Bo, Zhang Feng, Li Zhe
Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty.
NPJ genomic medicine 2021 12 6 (1): 107.
Saengkaew Tansit, Ruiz-Babot Gerard, David Alessia, Mancini Alessandra, Mariniello Katia, Cabrera Claudia P, Barnes Michael R, Dunkel Leo, Guasti Leonardo, Howard Sasha
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