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Results:
1-13
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Results: 13
Authors:
Wayne, S
Robertson, NG
DeClau, F
Chen, N
Verhoeven, K
Prasad, S
Tranebjarg, L
Morton, CC
Ryan, AF
Van Camp, G
Smith, RJH
Citation: S. Wayne et al., Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus, HUM MOL GEN, 10(3), 2001, pp. 195-200
Authors:
Verhoeven, K
Villanova, M
Rossi, A
Malandrini, A
De Jonghe, P
Timmerman, V
Citation: K. Verhoeven et al., Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1, AM J HU GEN, 69(4), 2001, pp. 889-894
Authors:
De Baere, E
Fukushima, Y
Small, K
Udar, N
Van Camp, G
Verhoeven, K
Palotie, A
De Paepe, A
Messiaen, L
Citation: E. De Baere et al., Identification of BPESC1, a novel gene disrupted by a balanced chromosomaltranslocation, t(3;4)(q23;p15.2), in a patient with BPES, GENOMICS, 68(3), 2000, pp. 296-304
Authors:
Verhoeven, K
Fagerheim, T
Prasad, S
Wayne, S
De Clau, F
Balemans, W
Verstreken, M
Schatteman, I
Solem, B
Van de Heyning, P
Tranebjarg, L
Smith, RJH
Van Camp, G
Citation: K. Verhoeven et al., Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment, HUM GENET, 107(1), 2000, pp. 7-11
Authors:
Verstreken, M
Declau, F
Schatteman, I
Van Velzen, D
Verhoeven, K
Van Camp, G
Willems, PJ
Kuhweide, EW
Verhaert, E
D'Haese, P
Wuyts, FL
Van de Heyning, PH
Citation: M. Verstreken et al., Audiometric analysis of a Belgian family linked to the DFNA10 locus, AM J OTOL, 21(5), 2000, pp. 675-681
Authors:
Van Camp, G
Coucke, PJ
Van Hauwe, P
Van Laer, L
Verhoeven, K
Wuyts, F
Smith, RJH
Citation: G. Van Camp et al., DFNA 2, 5, 8, 12, ADV OTO-RH, 56, 2000, pp. 68-77
Authors:
Auer-Grumbach, M
De Jonghe, P
Wagner, K
Verhoeven, K
Hartung, HP
Timmerman, V
Citation: M. Auer-grumbach et al., Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locus, NEUROLOGY, 55(10), 2000, pp. 1552-1557
Authors:
Verhoeven, K
Citation: K. Verhoeven, Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment (vol 19, pg 60, 1998), NAT GENET, 21(4), 1999, pp. 449-449
Authors:
Alloisio, N
Morle, L
Bozon, M
Godet, J
Verhoeven, K
Van Camp, G
Plauchu, H
Muller, P
Collet, L
Lina-Granade, G
Citation: N. Alloisio et al., Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss, EUR J HUM G, 7(2), 1999, pp. 255-258
Authors:
Verhoeven, K
Ensink, RJH
Tiranti, V
Huygen, PLM
Johnson, DF
Schatteman, I
Van Laer, L
Verstreken, M
Van de Heyning, P
Fischel-Ghodsian, N
Zeviani, M
Cremers, CWRJ
Willems, PJ
Van Camp, G
Citation: K. Verhoeven et al., Hearing impairment and neurological dysfunction associated with a mutationin the mitochondrial tRNA(Ser(UCN)) gene, EUR J HUM G, 7(1), 1999, pp. 45-51
Authors:
Balciuniene, J
Dahl, N
Jalonen, P
Verhoeven, K
Van Camp, G
Borg, E
Pettersson, U
Jazin, EE
Citation: J. Balciuniene et al., Alpha-tectorin involvement in hearing disabilities: one gene two phenotypes, HUM GENET, 105(3), 1999, pp. 211-216
Authors:
Van Den Bosch, L
Verhoeven, K
De Smedt, H
Wuytack, F
Missiaen, L
Robberecht, W
Citation: L. Van Den Bosch et al., Calcium handling proteins in isolated spinal motoneurons, LIFE SCI, 65(15), 1999, pp. 1597-1606
Authors:
Govaerts, PJ
De Ceulaer, G
Daemers, K
Verhoeven, K
Van Camp, G
Schatteman, I
Verstreken, M
Willems, PJ
Somers, T
Offeciers, FE
Citation: Pj. Govaerts et al., A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic,midfrequency, prelingual and nonprogressive sensorineural hearing loss, AM J OTOL, 19(6), 1998, pp. 718-723
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