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Results: 1-12 |
Results: 12

Authors: Cremers, C Bouamrane, F Singleton, L Schenk, R
Citation: C. Cremers et al., SU-8 as resist material for deep X-ray lithography, MICROSYST T, 7(1), 2001, pp. 11-16

Authors: Wagenaar, M Schuknecht, H Nadol, J Benraad-van Rens, M Pieke-Dahl, S Kimberling, W Cremers, C
Citation: M. Wagenaar et al., Histopathologic features of the temporal bone in Usher syndrome type I, ARCH OTOLAR, 126(8), 2000, pp. 1018-1023

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: Kupka, RK Bouamrane, F Cremers, C Megtert, S
Citation: Rk. Kupka et al., Microfabrication: LIGA-X and applications, APPL SURF S, 164, 2000, pp. 97-110

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: Wagenaar, M van Aarem, A Huygen, P Pieke-Dahl, S Kimberling, W Cremers, C
Citation: M. Wagenaar et al., Hearing impairment related to age in Usher syndrome types 1B and 2A, ARCH OTOLAR, 125(4), 1999, pp. 441-445

Authors: van Aarem, A Wagenaar, M Tonnaer, E Dahl, SP Bisseling, J Janssen, H Bastiaans, B Kimberling, W Cremers, C
Citation: A. Van Aarem et al., Semen analysis in the Usher syndrome type 2A, ORL-J OTO R, 61(3), 1999, pp. 126-130

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: Wagenaar, M Draaijer, P Meek, H ten Donkelaar, HJ Wesseling, P Kimberling, W Cremers, C
Citation: M. Wagenaar et al., The cochlear nuclei in two patients with Usher syndrome type I, INT J PED O, 50(3), 1999, pp. 185-195

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

Authors: Tashtoush, G Saito, K Cremers, C Gritzo, L
Citation: G. Tashtoush et al., Study of flame spread over JP8 using 2-D holographic interferometry, J FIRE SCI, 16(6), 1998, pp. 437-457
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