Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: PSMC3IP[original query] |
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Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. Journal of assisted reproduction and genetics 0 25 (11-12): 553-7. Miyamoto Toshinobu, Koh Eitetsu, Sakugawa Naoko, Sato Hisashi, Hayashi Hiroaki, Namiki Mikio, Sengoku Kaz |
Inactivating Mutations in GT198 in Familial and Early-Onset Breast and Ovarian Cancers. Genes & cancer 2013 Jan 4 (1-2): 15-25. Peng Min, Bakker Janine L, Dicioccio Richard A, Gille Johan J P, Zhao Hua, Odunsi Kunle, Sucheston Lara, Jaafar Lahcen, Mivechi Nahid F, Waisfisz Quinten, Ko L |
No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2014 8 (4): 146-50. Norling A, Hirschberg A L, Karlsson L, Rodriguez-Wallberg K A, Iwarsson E, Wedell A, Barbaro |
Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency. Journal of assisted reproduction and genetics 2018 11 36 (1): 39-45. Yang Xiang, Touraine Philippe, Desai Swapna, Humphreys Gregory, Jiang Huaiyang, Yatsenko Alexander, Rajkovic Aleksand |
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- Page last updated:Apr 22, 2024
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