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Alport syndrome--clinical phenotypes, incidence, and pathology.
Gregory MC, Terreros DA, Barker DF, Fain PN, Denison JC, Atkin CL. Gregory MC, et al. Among authors: denison jc. Contrib Nephrol. 1996;117:1-28. doi: 10.1159/000424804. Contrib Nephrol. 1996. PMID: 8801040 Review. No abstract available.
Molecular testing for adult type Alport syndrome.
Pont-Kingdon G, Sumner K, Gedge F, Miller C, Denison J, Gregory M, Lyon E. Pont-Kingdon G, et al. BMC Nephrol. 2009 Nov 17;10:38. doi: 10.1186/1471-2369-10-38. BMC Nephrol. 2009. PMID: 19919694 Free PMC article.
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
Heath KE, Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, Greinacher A, Epstein CJ, Glucksman MJ, Martignetti JA. Heath KE, et al. Among authors: denison jc. Am J Hum Genet. 2001 Nov;69(5):1033-45. doi: 10.1086/324267. Epub 2001 Oct 4. Am J Hum Genet. 2001. PMID: 11590545 Free PMC article.