Authors:
Kunst, H
Marres, H
Huygen, P
Van Duijnhoven, G
Krebsova, A
Van der Velde, S
Reis, A
Cremers, F
Cremers, C
Citation: H. Kunst et al., Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21), CLIN OTOLAR, 25(1), 2000, pp. 45-54
Authors:
Kunst, H
Huybrechts, C
Marres, H
Huygen, P
Van Camp, G
Cremers, C
Citation: H. Kunst et al., The phenotype of DFNA13/COL11A2: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment, AM J OTOL, 21(2), 2000, pp. 181-187
Authors:
Weston, MD
Eudy, JD
Fujita, S
Yao, SF
Usami, S
Cremers, C
Greenburg, J
Ramesar, R
Martini, A
Moller, C
Smith, RJ
Sumegi, J
Kimberling, WJ
Citation: Md. Weston et al., Genomic structure and identification of novel mutations in Usherin, the gene responsible for Usher syndrome type IIa, AM J HU GEN, 66(4), 2000, pp. 1199-1210
Authors:
Declau, F
Cremers, C
Van de Heyning, P
Amadori, M
Casselman, J
Causse, JB
Charachon, R
Granstrom, G
Martini, A
Offeciers, E
Somers, T
Tos, M
Citation: F. Declau et al., Diagnosis and management strategies in congenital atresia of the external auditory canal, BR J AUDIOL, 33(5), 1999, pp. 313-327
Authors:
Kunst, H
Marres, H
Huygen, P
Van Camp, G
Joosten, F
Cremers, C
Citation: H. Kunst et al., Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): Statistical analysis of hearing threshold in relation to age and evaluation of vestibule-ocular functions, AUDIOLOGY, 38(3), 1999, pp. 165-173