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Page 1
Hereditary intrinsic factor deficiency in chaldeans.
Sturm AC, Baack EC, Armstrong MB, Schiff D, Zia A, Savasan S, de la Chapelle A, Tanner SM. Sturm AC, et al. Among authors: tanner sm. JIMD Rep. 2013;7:13-8. doi: 10.1007/8904_2012_133. Epub 2012 Mar 18. JIMD Rep. 2013. PMID: 23430489 Free PMC article.
Familial peripheral keratopathy without PAX6 mutation.
Smith WM, Lange JM, Sturm AC, Tanner SM, Mauger TF. Smith WM, et al. Among authors: tanner sm. Cornea. 2012 Feb;31(2):130-3. doi: 10.1097/ICO.0b013e3182222779. Cornea. 2012. PMID: 22146551
Imerslund-Gräsbeck syndrome: new mutation in amnionless.
Densupsoontorn N, Sanpakit K, Vijarnsorn C, Pattaragarn A, Kangwanpornsiri C, Jatutipsompol C, Tirapongporn H, Jirapinyo P, Shah NP, Sturm AC, Tanner SM. Densupsoontorn N, et al. Among authors: tanner sm. Pediatr Int. 2012 Jun;54(3):e19-21. doi: 10.1111/j.1442-200X.2011.03482.x. Pediatr Int. 2012. PMID: 22631584 No abstract available.
Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia.
Raval A, Tanner SM, Byrd JC, Angerman EB, Perko JD, Chen SS, Hackanson B, Grever MR, Lucas DM, Matkovic JJ, Lin TS, Kipps TJ, Murray F, Weisenburger D, Sanger W, Lynch J, Watson P, Jansen M, Yoshinaga Y, Rosenquist R, de Jong PJ, Coggill P, Beck S, Lynch H, de la Chapelle A, Plass C. Raval A, et al. Among authors: tanner sm. Cell. 2007 Jun 1;129(5):879-90. doi: 10.1016/j.cell.2007.03.043. Cell. 2007. PMID: 17540169 Free PMC article.
78 results