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