Citation: H. Kunst et al., NON-SYNDROMIC AUTOSOMAL-DOMINANT SENSORINEURAL HEARING-LOSS - A NEW FIELD OF RESEARCH, Clinical otolaryngology and allied sciences, 23(1), 1998, pp. 9-17
Authors:
EUDY JD
WESTON MD
YAO SF
HOOVER DM
REHM HL
MAEDMONDS M
YAN D
AHMAD I
CHENG JJ
AYUSO C
CREMERS C
DAVENPORT S
MOLLER C
TALMADGE CB
BEISEL KW
TAMAYO M
MORTON CC
SWAROOP A
KIMBERLING WJ
SUMEGI J
Citation: Jd. Eudy et al., MUTATION OF A GENE ENCODING A PROTEIN WITH EXTRACELLULAR-MATRIX MOTIFS IN USHER-SYNDROME TYPE-IIA, Science, 280(5370), 1998, pp. 1753-1757
Authors:
KUNST H
MARRES H
HUYGEN P
ENSINK R
VANCAMP G
VANHAUWE P
COUCKE P
WILLEMS P
CREMERS C
Citation: H. Kunst et al., NONSYNDROMIC AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS - AUDIOLOGICAL ANALYSIS OF A PEDIGREE LINKED TO DFNA2, The Laryngoscope, 108(1), 1998, pp. 74-80
Citation: C. Cremers et J. Degen, SPECTROSCOPIC EVIDENCE FOR THE COEXISTENCE OF TETRAGONAL AND TRIGONALMINIMA WITHIN THE EXITED STATE ADIABATIC POTENTIAL-ENERGY SURFACES OFHEXACHLOROTELLURATE AND HEXACHLORO-SELENATE COMPLEXES, The Journal of chemical physics, 109(19), 1998, pp. 8521-8526
Authors:
MARRES H
VANEWIJK M
HUYGEN P
KUNST H
VANCAMP G
COUCKE P
WILLEMS P
CREMERS C
Citation: H. Marres et al., INHERITED NONSYNDROMIC HEARING-LOSS - AN AUDIOVESTIBULAR STUDY IN A LARGE FAMILY WITH AUTOSOMAL-DOMINANT PROGRESSIVE HEALING LOSS RELATED TO DFNA2, Archives of otolaryngology, head & neck surgery, 123(6), 1997, pp. 573-577
Authors:
STINCKENS C
ENSINK R
FEENSTRA L
FRYNS JP
CREMERS C
Citation: C. Stinckens et al., NON-SYNDROMIC DOMINANT SENSORINEURAL HEARING-LOSS - FROM A FEW PHENOTYPES TO MANY GENOTYPES, International journal of pediatric otorhinolaryngology, 38(3), 1997, pp. 237-245
Authors:
WESTON MD
KELLEY PM
OVERBECK LD
WAGENAAR M
ORTEN DJ
HASSON T
CHEN ZY
COREY D
MOOSEKER M
SUMEGI J
CREMERS C
MOLLER C
JACOBSON SG
GORIN MB
KIMBERLING WJ
Citation: Md. Weston et al., MYOSIN VIIA MUTATION SCREENING IN 189-USHER-SYNDROME TYPE-1 PATIENTS, American journal of human genetics, 59(5), 1996, pp. 1074-1083
Authors:
WAGENAAR M
TERRAHE B
VANAAREM A
HUYGEN P
ADMIRAAL R
BLEEKERWAGEMAKERS E
PINCKERS A
KIMBERLING W
CREMERS C
Citation: M. Wagenaar et al., CLINICAL FINDINGS IN OBLIGATE CARRIERS OF TYPE-I USHER SYNDROME, American journal of medical genetics, 59(3), 1995, pp. 375-379