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Results: 1-4 |
Results: 4

Authors: Hart, TC Hart, PS Michalec, MD Zhang, Y Firatli, E Van Dyke, TE Stabholz, A Zlorogorski, A Shapira, L Soskolne, WA
Citation: Tc. Hart et al., Haim-Munk syndrome and Papillon-Lefevre syndrome are allelic mutations in cathepsin C, J MED GENET, 37(2), 2000, pp. 88-94

Authors: Hart, TC Hart, PS Michalec, MD Zhang, Y Marazita, ML Cooper, M Yassin, OM Nusier, M Walker, S
Citation: Tc. Hart et al., Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation, J MED GENET, 37(2), 2000, pp. 95-101

Authors: Hart, PS Zhang, Y Firatli, E Uygur, C Lotfazar, M Michalec, MD Marks, JJ Lu, X Coates, BJ Seow, WK MarshaIl, R Williams, D Reed, JB Wright, JT Hart, TC
Citation: Ps. Hart et al., Identification of cathepsin C mutations in ethnically diverse Papillon-Lefevre syndrome patients, J MED GENET, 37(12), 2000, pp. 927-932

Authors: Hart, TC Hart, PS Bowden, DW Michalec, MD Callison, SA Walker, SJ Zhang, YZ Firatli, E
Citation: Tc. Hart et al., Mutations of the cathepsin C gene are responsible for Papillon-Lefevre syndrome, J MED GENET, 36(12), 1999, pp. 881-887
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