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Results: 1-9 |
Results: 9

Authors: KUNST H MARRES H VANCAMP G CREMERS C
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

Authors: CREMERS C DEGEN J
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

Authors: KIMBERLING WJ WESTON MD MOLLER C CREMERS C MARTINI A AYUSO C TOMAYO M SUMEGI J CONNOLLY C FOWLER T HOOVER D
Citation: Wj. Kimberling et al., MAPPING USHER TYPE IIA TO CHROMOSOME 1Q41, Cytogenetics and cell genetics, 67(3), 1994, pp. 170-170
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