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A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.
Walls WD, Moteki H, Thomas TR, Nishio SY, Yoshimura H, Iwasa Y, Frees KL, Nishimura CJ, Azaiez H, Booth KT, Marini RJ, Kolbe DL, Weaver AM, Schaefer AM, Wang K, Braun TA, Usami SI, Barr-Gillespie PG, Richardson GP, Smith RJ, Casavant TL. Walls WD, et al. Hum Genet. 2020 Oct;139(10):1315-1323. doi: 10.1007/s00439-020-02174-y. Epub 2020 May 7. Hum Genet. 2020. PMID: 32382995 Free PMC article.
De novo variants are a common cause of genetic hearing loss.
Klimara MJ, Nishimura C, Wang D, Kolbe DL, Schaefer AM, Walls WD, Frees KL, Smith RJH, Azaiez H. Klimara MJ, et al. Among authors: walls wd. Genet Med. 2022 Dec;24(12):2555-2567. doi: 10.1016/j.gim.2022.08.028. Epub 2022 Oct 4. Genet Med. 2022. PMID: 36194208 Free PMC article.
Early investigation of haematemesis and melaena.
Walls WD, Glanville JN, Chandler GN. Walls WD, et al. Lancet. 1971 Aug 21;2(7721):387-90. doi: 10.1016/s0140-6736(71)90110-3. Lancet. 1971. PMID: 4105170 Clinical Trial. No abstract available.
20 results