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Results: 1-5 |
Results: 5

Authors: Robinson, WP Christian, SL Kuchinka, BD Penaherrera, S Das, S Schuffenhauer, S Malcolm, S Schinzel, AA Hassold, TJ Ledbetter, DH
Citation: Wp. Robinson et al., Somatic segregation errors predominantly contribute to the gain or loss ofa paternal chromosome leading to uniparental disomy for chromosome 15, CLIN GENET, 57(5), 2000, pp. 349-358

Authors: Salam, AA Hafner, FM Linder, TE Spillmann, T Schinzel, AA Leal, SM
Citation: Aa. Salam et al., A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic heaving loss maps to 14q21-q22 in a Swiss German kindred, AM J HU GEN, 66(6), 2000, pp. 1984-1988

Authors: Hafner, FM Salam, AA Linder, TE Balmer, D Baumer, A Schinzel, AA Spillmann, T Leal, SM
Citation: Fm. Hafner et al., A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred, AM J HU GEN, 66(4), 2000, pp. 1437-1442

Authors: Blagitko, N Schulz, U Schinzel, AA Ropers, HH Kalscheuer, VM
Citation: N. Blagitko et al., gamma 2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome, HUM MOL GEN, 8(13), 1999, pp. 2387-2396

Authors: Kohlhase, J Taschner, PEM Burfeind, P Pasche, B Newman, B Blanck, C Breuning, MH ten Kate, LP Maaswinkel-Mooy, P Mitulla, B Seidel, J Kirkpatrick, SJ Pauli, RM Wargowski, DS Devriendt, K Proesmans, W Gabrielli, O Coppa, GV Wesby-van Swaay, E Trembath, RC Schinzel, AA Reardon, W Seemanova, E Engel, W
Citation: J. Kohlhase et al., Molecular analysis of SALL1 mutations in Townes-Brocks syndrome, AM J HU GEN, 64(2), 1999, pp. 435-445
Risultati: 1-5 |