Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Cryptorchidism and FGF8[original query] |
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Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies. Birth defects research. Part A, Clinical and molecular teratology 2014 Oct 100 (10): 750-9. Zeidler Claudia, Woelfle Joachim, Draaken Markus, Mughal Sadaf S, Große Greta, Hilger Alina C, Dworschak Gabriel C, Boemers Thomas M, Jenetzky Ekkehart, Zwink Nadine, Lacher Martin, Schmidt Dominik, Schmiedeke Eberhard, Grasshoff-Derr Sabine, Märzheuser Stefanie, Holland-Cunz Stefan, Schäfer Mattias, Bartels Enrika, Keppler Kathleen, Palta Markus, Leonhardt Johannes, Kujath Christina, Rißmann Anke, Nöthen Markus M, Reutter Heiko, Ludwig Micha |
Genetics of congenital hypogonadotropic hypogonadism in Denmark. European journal of medical genetics 2014 Jul 57 (7): 345-8. Tommiska Johanna, Känsäkoski Johanna, Christiansen Peter, Jørgensen Niels, Lawaetz Jacob Gerner, Juul Anders, Raivio Tane |
Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism. Journal of medical genetics 2020 5 58 (1): 66-72. Men Meichao, Wang Xinying, Wu Jiayu, Zeng Wang, Jiang Fang, Zheng Ruizhi, Li Jia- |
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