Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: EXOSC3[original query] |
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Pathway analysis of a genome-wide association study in schizophrenia. Gene 2013 Aug 525 (1): 107-15. Lee Young Ho, Kim Jae-Hoon, Song Gwan G |
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations. Orphanet journal of rare diseases 2014 9 (1): 23. Eggens Veerle Rc, Barth Peter G, Niermeijer Jikke-Mien F, Berg Jonathan N, Darin Niklas, Dixit Abhijit, Fluss Joel, Foulds Nicola, Fowler Darren, Hortobágyi Tibor, Jacques Thomas, King Mary D, Makrythanasis Periklis, Máté Adrienn, Nicoll James A R, O'Rourke Declan, Price Sue, Williams Andrew N, Wilson Louise, Suri Mohnish, Sztriha Laszlo, Dijns-de Wissel Marit B, van Meegen Mia T, van Ruissen Fred, Aronica Eleonora, Troost Dirk, Majoie Charles Blm, Marquering Henk A, Poll-Thé Bwee Tien, Baas Fra |
Atypical haemolytic uraemic syndrome in the era of terminal complement inhibition- An observational cohort study. Blood 2023 6 . Vicky Brocklebank, Patrick R Walsh, Kate Smith-Jackson, Thomas M Hallam, Kevin J Marchbank, Valerie Wilson, Theophile Bigirumurame, Tina Dutt, Emma K Montgomery, Michal Malina, Edwin Ks Wong, Sally Johnson, Neil Sheerin, David Kavana |
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