Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: UPF2[original query] |
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Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders. Human molecular genetics 2013 Jan . Nguyen LS, Kim HG, Rosenfeld JA, Shen Y, Gusella JF, Lacassie Y, Layman LC, Shaffer LG, Gecz J |
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism. BMC urology 2016 Oct 16 (1): 62. Wang Yanping, Li Jin, Kolon Thomas F, Olivant Fisher Alicia, Figueroa T Ernesto, BaniHani Ahmad H, Hagerty Jennifer A, Gonzalez Ricardo, Noh Paul H, Chiavacci Rosetta M, Harden Kisha R, Abrams Debra J, Stabley Deborah, Kim Cecilia E, Sol-Church Katia, Hakonarson Hakon, Devoto Marcella, Barthold Julia Spenc |
De novo mutations in idiopathic male infertility-A pilot study. Andrology 2020 8 9 (1): 212-220. Hodži? Alenka, Maver Aleš, Plaseska-Karanfilska Dijana, Ristanovi? Mom?ilo, Noveski Predrag, Zorn Branko, Terzic Marija, Kunej Tanja, Peterlin Bor |
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