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Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.
Williamson KA, Rainger J, Floyd JA, Ansari M, Meynert A, Aldridge KV, Rainger JK, Anderson CA, Moore AT, Hurles ME, Clarke A, van Heyningen V, Verloes A, Taylor MS, Wilkie AO; UK10K Consortium; Fitzpatrick DR. Williamson KA, et al. Among authors: aldridge kv. Am J Hum Genet. 2014 Feb 6;94(2):295-302. doi: 10.1016/j.ajhg.2014.01.001. Epub 2014 Jan 23. Am J Hum Genet. 2014. PMID: 24462371 Free PMC article.
Prospective study of respiratory infections at the U.S. Naval Academy.
Gray GC, Schultz RG, Gackstetter GD, McKeehan JA, Aldridge KV, Hudspeth MK, Malasig MD, Fuller JM, McBride WZ. Gray GC, et al. Among authors: aldridge kv. Mil Med. 2001 Sep;166(9):759-63. doi: 10.1093/milmed/166.9.759. Mil Med. 2001. PMID: 11569436