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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: Counseling and PROKR2[original query]
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
European journal of endocrinology / European Federation of Endocrine Societies 2013 Dec 169 (6): 805-9.
Sarfati Julie, Fouveaut Corinne, Leroy Chrystel, Jeanpierre Marc, Hardelin Jean-Pierre, Dodé Catheri
Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.
The Journal of clinical endocrinology and metabolism 2013 Mar 98 (3): E547-57.
McCabe Mark J, Gaston-Massuet Carles, Gregory Louise C, Alatzoglou Kyriaki S, Tziaferi Vaitsa, Sbai Oualid, Rondard Philippe, Masumoto Koh-hei, Nagano Mamoru, Shigeyoshi Yasufumi, Pfeifer Marija, Hulse Tony, Buchanan Charles R, Pitteloud Nelly, Martinez-Barbera Juan-Pedro, Dattani Mehul
Correlations Among Genotype and Outcome in Chinese Male Patients With Congenital Hypogonadotropic Hypogonadism Under HCG Treatment.
The journal of sexual medicine 2020 3 17 (4): 645-657.
Chen Yinwei, Sun Taotao, Niu Yonghua, Wang Daoqi, Xiong Zhiyong, Li Chuanzhou, Liu Kang, Qiu Youlan, Sun Yi, Gong Jianan, Wang Tao, Wang Shaogang, Xu Hao, Liu Jiho
[Analysis of a patient with Kallmann syndrome and a 45,X/46,XY karyotype].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 11 39 (11): 1275-1278.
Ma Fuhui, Wang Xinling, Reziwanguli Wusiman, Chen Yuan, Guo Yanyi
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