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Chronic granulomatous disease. Report on a national registry of 368 patients.
Winkelstein JA, Marino MC, Johnston RB Jr, Boyle J, Curnutte J, Gallin JI, Malech HL, Holland SM, Ochs H, Quie P, Buckley RH, Foster CB, Chanock SJ, Dickler H. Winkelstein JA, et al. Among authors: chanock sj. Medicine (Baltimore). 2000 May;79(3):155-69. doi: 10.1097/00005792-200005000-00003. Medicine (Baltimore). 2000. PMID: 10844935 Free article.
SNPing away at innate immunity.
Chanock SJ, Foster CB. Chanock SJ, et al. J Clin Invest. 1999 Aug;104(4):369-70. doi: 10.1172/JCI7986. J Clin Invest. 1999. PMID: 10449427 Free PMC article. Review. No abstract available.
Genomic structure of the human p47-phox (NCF1) gene.
Chanock SJ, Roesler J, Zhan S, Hopkins P, Lee P, Barrett DT, Christensen BL, Curnutte JT, Görlach A. Chanock SJ, et al. Blood Cells Mol Dis. 2000 Feb;26(1):37-46. doi: 10.1006/bcmd.2000.0274. Blood Cells Mol Dis. 2000. PMID: 10772875
Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease: The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes.
Vázquez N, Lehrnbecher T, Chen R, Christensen BL, Gallin JI, Malech H, Holland S, Zhu S, Chanock SJ. Vázquez N, et al. Among authors: chanock sj. Exp Hematol. 2001 Feb;29(2):234-43. doi: 10.1016/s0301-472x(00)00646-9. Exp Hematol. 2001. PMID: 11166463 Free article.
Using genetic variation to study human disease.
Taylor JG, Choi EH, Foster CB, Chanock SJ. Taylor JG, et al. Among authors: chanock sj. Trends Mol Med. 2001 Nov;7(11):507-12. doi: 10.1016/s1471-4914(01)02183-9. Trends Mol Med. 2001. PMID: 11689336 Review.
1,010 results