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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 1, 2023. (Total: 221588Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Cryptorchidism and LGR8[original query]
Lack of LGR8 gene mutation in Finnish patients with a family history of cryptorchidism.
Reproductive biomedicine online 0 7 (4): 400-6.
Roh Jaesook, Virtanen Helena, Kumagai Jin, Sudo Satoko, Kaleva Marko, Toppari Jorma, Hsueh Aaron J
Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: clinical and functional characterization.
Molecular human reproduction 2006 Jun 12 (6): 401-6.
Ferlin A, Bogatcheva N V, Gianesello L, Pepe A, Vinanzi C, Agoulnik A I, Foresta
Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism.
Hormone research 2007 67 (2): 73-6.
Yamazawa Kazuki, Wada Yuka, Sasagawa Isoji, Aoki Katsuya, Ueoka Katsuhiko, Ogata Tsuto
Novel mutations involving the INSL3 gene associated with cryptorchidism.
The Journal of urology 2007 May 177 (5): 1947-51.
El Houate Brahim, Rouba Hassan, Sibai Hicham, Barakat Abdelhamid, Chafik Abdelaziz, Chadli El Bekkay, Imken Laila, Bogatcheva Natalia V, Feng Shu, Agoulnik Alexander I, McElreavey K
The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism.
The Journal of clinical endocrinology and metabolism 2008 Mar 93 (3): 1072-6.
Nuti Francesca, Marinari Eliana, Erdei Edit, El-Hamshari Manal, Echavarria Mirna Guadalupe, Ars Elisabet, Balercia Giancarlo, Merksz Miklos, Giachini Claudia, Shaeer Kamal Zaki Mahmoud, Forti Gianni, Ruiz-Castané Eduard, Krausz Csil
No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population.
Hormone research 2008 70 (4): 236-9.
El Houate Brahim, Rouba Hassan, Imken Laila, Sibai Hicham, Chafik Abdelaziz, Boulouiz Redouane, Chadli Elbakkay, Hassar Mohmmed, McElreavey Ken, Barakat Abdelham
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