A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment
VAN LAER, L, COUCKE, P, FRANSEN, E, ROWLAND, J, CUCCI, R. A, SMITH, R. J. H, VAN CAMP, G, MUELLER, R. F, CAETHOVEN, G, FLOTHMANN, K, PRASAD, S. D, CHAMBERLIN, G. P, HOUSEMAN, M, TAYLOR, G. R, VAN DE HEYNING, C. M
Published in Journal of medical genetics (01.08.2001)
Published in Journal of medical genetics (01.08.2001)
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EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas
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Published in American journal of human genetics (01.09.1999)
Published in American journal of human genetics (01.09.1999)
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A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36
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Published in American journal of human genetics (01.02.2001)
Published in American journal of human genetics (01.02.2001)
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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
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Published in Human genetics (01.05.2002)
Published in Human genetics (01.05.2002)
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A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13
Ensink, R.J.H., Huygen, P.L.M., Snoeckx, R.L., Caethoven, G., Van Camp, G., Cremers, C.W.R.J.
Published in Clinical otolaryngology and allied sciences (01.08.2001)
Published in Clinical otolaryngology and allied sciences (01.08.2001)
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A novel Z-score-based method to analyze candidate genes for age-related hearing impairment
Fransen, Erik, Van Laer, Lut, Lemkens, Nele, Caethoven, Goele, Flothmann, Kris, Govaerts, Paul, Van de Heyning, Paul, Van Camp, Guy
Published in Ear and hearing (01.04.2004)
Published in Ear and hearing (01.04.2004)
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A dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13
Ensink, R J H, Huygen, P L M, Snoeckk, R L, Caethoven, G
Published in Clinical otolaryngology (01.08.2001)
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Published in Clinical otolaryngology (01.08.2001)
Journal Article
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment
Van Laer, L, Coucke, P, Mueller, R F, Caethoven, G, Flothmann, K, Prasad, S D, Chamberlin, G P, Houseman, M, Taylor, G R, Van de Heyning, C M, Fransen, E, Rowland, J, Cucci, R A, Smith, R J H, Van Camp, G
Published in Journal of medical genetics (01.08.2001)
Published in Journal of medical genetics (01.08.2001)
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