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Results: 1-5 |
Results: 5

Authors: Omran, H Haffner, KN Burth, S Ala-Mello, S Antignac, C Hildebrandt, F
Citation: H. Omran et al., Evidence for further genetic heterogeneity in nephronophthisis, NEPH DIAL T, 16(4), 2001, pp. 755-758

Authors: Ala-Mello, S Kaariainen, H Koskimies, O
Citation: S. Ala-mello et al., Nephronophthisis and ulcerative colitis in siblings: a new association, PED NEPHROL, 16(6), 2001, pp. 507-509

Authors: Auranen, M Ala-Mello, S Turunen, JA Jarvela, I
Citation: M. Auranen et al., Further evidence for linkage of autosomal-dominant medullary cystic kidneydisease on chromosome 1q21, KIDNEY INT, 60(4), 2001, pp. 1225-1232

Authors: Ala-Mello, S Koskimies, O Rapola, J Kaariainen, H
Citation: S. Ala-mello et al., Nephronophthisis in Finland: epidemiology and comparison of genetically classified subgroups, EUR J HUM G, 7(2), 1999, pp. 205-211

Authors: McIntosh, I Dreyer, SD Clough, MV Dunston, JA Eyaid, W Roig, CM Montgomery, T Ala-Mello, S Kaitila, I Winterpacht, A Zabel, B Frydman, M Cole, WG Francomano, CA Lee, B
Citation: I. Mcintosh et al., Mutation analysis of LMX1B gene in nail-patella syndrome patients, AM J HU GEN, 63(6), 1998, pp. 1651-1658
Risultati: 1-5 |