Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 21, 2023. (Total: 221327Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 3 (of 3 Records)

Query Trace: Cryptorchidism and GNRHR[original query]
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
The Journal of clinical endocrinology and metabolism 2008 Oct 93 (10): 4113-8.
Abreu Ana Paula, Trarbach Ericka Barbosa, de Castro Margaret, Frade Costa Elaine Maria, Versiani Beatriz, Matias Baptista Maria Tereza, Garmes Heraldo Mendes, Mendonca Berenice Bilharinho, Latronico Ana Claud
Isolated cryptorchidism: no evidence for involvement of genes underlying isolated hypogonadotropic hypogonadism.
Molecular and cellular endocrinology 2011 Jul 341 (1-2): 35-8.
Laitinen Eeva-Maria, Tommiska Johanna, Virtanen Helena E, Oehlandt Heidi, Koivu Rosanna, Vaaralahti Kirsi, Toppari Jorma, Raivio Tane
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
TOP