Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and WNT4[original query] |
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Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women. Reproductive biomedicine online 2012 Jun 24 (6): 630-3. Chang Xinyue, Qin Yingying, Xu Chengyan, Li Guangyu, Zhao Xiaoming, Chen Zi-Jia |
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han. PloS one 2015 10 (6): e0130202. Ma Wenqing, Li Ya, Wang Man, Li Haixia, Su Tiefen, Li Yan, Wang Shixu |
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia. Molecular cytogenetics 2018 2 11 13. Demir Eksi Durkadin, Shen Yiping, Erman Munire, Chorich Lynn P, Sullivan Megan E, Bilekdemir Meric, Y?lmaz Elanur, Luleci Guven, Kim Hyung-Goo, Alper Ozgul M, Layman Lawrence |
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
Communications biology 2020 Mar 3 (1): 129. Olafsdottir Thorhildur, Thorleifsson Gudmar, Sulem Patrick, Stefansson Olafur A, Medek Helga, Olafsson Karl, Ingthorsson Orri, Gudmundsson Valur, Jonsdottir Ingileif, Halldorsson Gisli H, Kristjansson Ragnar P, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Oddsson Asmundur, Sigurdsson Asgeir, Eggertsson Hannes P, Melsted Pall, Halldorsson Bjarni V, Lund Sigrun H, Styrkarsdottir Unnur, Steinthorsdottir Valgerdur, Gudmundsson Julius, Holm Hilma, Tragante Vinicius, Asselbergs Folkert W, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Jonsdottir Kristin, Rafnar Thorunn, Stefansson Ka |
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