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Results: 1-25 | 26-50 | 51-75 | 76-81
Results: 1-25/81
IDENTIFICATION OF 3 NOVEL MUTATIONS IN HUMAN EYA1 PROTEIN ASSOCIATED WITH BRANCHIOOTORENAL SYNDROME
Authors: KUMAR S KIMBERLING WJ WESTON MD SCHAEFER BG BERG MA MARRES HAM CREMERS CWRJ
Citation: S. Kumar et al., IDENTIFICATION OF 3 NOVEL MUTATIONS IN HUMAN EYA1 PROTEIN ASSOCIATED WITH BRANCHIOOTORENAL SYNDROME, Human mutation, 11(6), 1998, pp. 443-449
IDENTIFICATION OF 2 PAX3 MUTATIONS CAUSING WAARDENBURG SYNDROME, ON WITHIN THE PAIRED DOMAIN (M62V) AND THE OTHER DOWNSTREAM OF THE HOMEODOMAIN (Q282X)
Authors: HOL FA GEURDS MPA CREMERS CWRJ HAMEL BCJ MARIMAN ECM
Citation: Fa. Hol et al., IDENTIFICATION OF 2 PAX3 MUTATIONS CAUSING WAARDENBURG SYNDROME, ON WITHIN THE PAIRED DOMAIN (M62V) AND THE OTHER DOWNSTREAM OF THE HOMEODOMAIN (Q282X), Human mutation, 1998, pp. 145-147
IDENTIFICATION OF 10 NOVEL MUTATIONS IN THE PDS GENE RESPONSIBLE FOR PENDRED-SYNDROME
Authors: VANHAUWE P EVERETT L COUCKE P CHEN A RIS C BOLDER C OTTEN B DEVIJLDER J SMITH RJH WILLEMS PJ CREMERS CWRJ GREEN ED VANCAMP G
Citation: P. Vanhauwe et al., IDENTIFICATION OF 10 NOVEL MUTATIONS IN THE PDS GENE RESPONSIBLE FOR PENDRED-SYNDROME, European journal of human genetics, 6, 1998, pp. 205-205
NON-ALLELIC GENETIC-HETEROGENEITY IN A FAMILY WITH NONSYNDROMAL DEAFNESS
Authors: KREMER H CREMERS CWRJ VANDENHELM B MARRES HAM MEERMAN GJT BLEIJS DA ROPERS HH MARIMAN ECM
Citation: H. Kremer et al., NON-ALLELIC GENETIC-HETEROGENEITY IN A FAMILY WITH NONSYNDROMAL DEAFNESS, European journal of human genetics, 6, 1998, pp. 4168-4168
2 FREQUENT MISSENSE MUTATIONS IN PENDRED-SYNDROME
Authors: VANHAUWE P EVERETT LA COUCKE P SCOTT DA KRAFT ML RISSTALPERS C BOLDER C OTTEN B DEVIJLDER JJM DIETRICH NL RAMESH A SRISAILAPATHY SCR PARVING A CREMERS CWRJ WILLEMS PJ SMITH RJH GREEN ED VANCAMP G
Citation: P. Vanhauwe et al., 2 FREQUENT MISSENSE MUTATIONS IN PENDRED-SYNDROME, Human molecular genetics (Print), 7(7), 1998, pp. 1099-1104
EARLY-ONSET SENSORINEURAL HEARING-LOSS AND LATE-ONSET NEUROLOGIC COMPLAINTS CAUSED BY A MITOCHONDRIAL MUTATION AT POSITION-74-72
Authors: ENSINK RJH VERHOEVEN K MARRES HAM HUYGEN PLM PADBERG GW TERLAAK H VANCAMP G WILLEMS PJ CREMERS CWRJ
Citation: Rjh. Ensink et al., EARLY-ONSET SENSORINEURAL HEARING-LOSS AND LATE-ONSET NEUROLOGIC COMPLAINTS CAUSED BY A MITOCHONDRIAL MUTATION AT POSITION-74-72, Archives of otolaryngology, head & neck surgery, 124(8), 1998, pp. 886-891
PROGRESSIVE SENSORINEURAL HEARING-LOSS AND A WIDENED VESTIBULAR AQUEDUCT IN PENDRED-SYNDROME
Authors: CREMERS CWRJ BOLDER C ADMIRAAL RJC EVERETT LA JOOSTEN FBM VANHAUWE P GREEN ED OTTEN BJ
Citation: Cwrj. Cremers et al., PROGRESSIVE SENSORINEURAL HEARING-LOSS AND A WIDENED VESTIBULAR AQUEDUCT IN PENDRED-SYNDROME, Archives of otolaryngology, head & neck surgery, 124(5), 1998, pp. 501-505
SHORT-AND LONG-TERM RESULTS WITH IMPLANTABLE TRANSCUTANEOUS AND PERCUTANEOUS BONE-CONDUCTION DEVICES
Authors: SNIK AFM DRESCHLER WA TANGE RA CREMERS CWRJ
Citation: Afm. Snik et al., SHORT-AND LONG-TERM RESULTS WITH IMPLANTABLE TRANSCUTANEOUS AND PERCUTANEOUS BONE-CONDUCTION DEVICES, Archives of otolaryngology, head & neck surgery, 124(3), 1998, pp. 265-268
INTRAINDIVIDUAL COMPARISON OF THE BONE-ANCHORED HEARING-AID AND AIR-CONDUCTION HEARING-AIDS
Authors: MYLANUS EAM VANDERPOUW KCTM SNIK AFM CREMERS CWRJ
Citation: Eam. Mylanus et al., INTRAINDIVIDUAL COMPARISON OF THE BONE-ANCHORED HEARING-AID AND AIR-CONDUCTION HEARING-AIDS, Archives of otolaryngology, head & neck surgery, 124(3), 1998, pp. 271-276
IMPLANTABLE HEARING DEVICES FOR SENSORINEURAL HEARING-LOSS - A REVIEWOF THE AUDIOMETRIC DATA
Authors: SNIK AFM MYLANUS EAM CREMERS CWRJ
Citation: Afm. Snik et al., IMPLANTABLE HEARING DEVICES FOR SENSORINEURAL HEARING-LOSS - A REVIEWOF THE AUDIOMETRIC DATA, Clinical otolaryngology and allied sciences, 23(5), 1998, pp. 414-419
MITOCHONDRIAL INHERITED HEARING-LOSS
Authors: ENSINK RJH CAMP GV CREMERS CWRJ
Citation: Rjh. Ensink et al., MITOCHONDRIAL INHERITED HEARING-LOSS, Clinical otolaryngology and allied sciences, 23(1), 1998, pp. 3-8
REMOVAL OF TITANIUM IMPLANTS FROM THE TEMPORAL BONE - HISTOLOGIC-FINDINGS
Authors: VANDERPOUW CTM JOHANSSON CB MYLANUS EAM ALBREKTSSON T CREMERS CWRJ
Citation: Ctm. Vanderpouw et al., REMOVAL OF TITANIUM IMPLANTS FROM THE TEMPORAL BONE - HISTOLOGIC-FINDINGS, The American journal of otology, 19(1), 1998, pp. 46-51
PROGRESSIVE HEARING-LOSS, HYPOPLASIA OF THE COCHLEA AND WIDENED VESTIBULAR AQUEDUCTS ARE VERY COMMON FEATURES IN PENDREDS-SYNDROME
Authors: CREMERS CWRJ ADMIRAAL RJC HUYGEN PLM BOLDER C EVERETT LA JOOSTEN FBM GREEN ED VANCAMP G OTTEN BJ
Citation: Cwrj. Cremers et al., PROGRESSIVE HEARING-LOSS, HYPOPLASIA OF THE COCHLEA AND WIDENED VESTIBULAR AQUEDUCTS ARE VERY COMMON FEATURES IN PENDREDS-SYNDROME, International journal of pediatric otorhinolaryngology, 45(2), 1998, pp. 113-123
THE VELO-CARDIO-FACIAL SYNDROME - THE OTORHINOLARYNGEAL MANIFESTATIONS AND IMPLICATIONS
Authors: VANTRAPPEN G ROMMEL N CREMERS CWRJ DEVRIENDT K FRIJNS JP
Citation: G. Vantrappen et al., THE VELO-CARDIO-FACIAL SYNDROME - THE OTORHINOLARYNGEAL MANIFESTATIONS AND IMPLICATIONS, International journal of pediatric otorhinolaryngology, 45(2), 1998, pp. 133-141
RECURRENT THERAPY-RESISTANT MASTOIDITIS BY MYCOBACTERIUM-CHEILONAE-ABSCESSUS, A NONTUBERCULOUS MYCOBACTERIUM
Authors: VANAAREM A MUYTJENS HL SMITS MM CREMERS CWRJ
Citation: A. Vanaarem et al., RECURRENT THERAPY-RESISTANT MASTOIDITIS BY MYCOBACTERIUM-CHEILONAE-ABSCESSUS, A NONTUBERCULOUS MYCOBACTERIUM, International journal of pediatric otorhinolaryngology, 43(1), 1998, pp. 61-72
AUTOSOMAL-DOMINANT BRANCHIO-OTIC (BO) SYNDROME IS NOT ALLELIC TO THE BRANCHIOOTORENAL (BOR) GENE AT 8Q13
Authors: KUMAR S MARRES HAM CREMERS CWRJ KIMBERLING WJ
Citation: S. Kumar et al., AUTOSOMAL-DOMINANT BRANCHIO-OTIC (BO) SYNDROME IS NOT ALLELIC TO THE BRANCHIOOTORENAL (BOR) GENE AT 8Q13, American journal of medical genetics, 76(5), 1998, pp. 395-401
A NEW MORE POWERFUL BONE-ANCHORED HEARING-AID - FIRST RESULTS
Authors: VANDERPOUW CTM CARLSSON P CREMERS CWRJ SNIK AFM
Citation: Ctm. Vanderpouw et al., A NEW MORE POWERFUL BONE-ANCHORED HEARING-AID - FIRST RESULTS, Scandinavian audiology, 27(3), 1998, pp. 179-182
AUDIOMETRIC RESULTS OF BILATERAL BONE-ANCHORED HEARING-AID APPLICATION IN PATIENTS WITH BILATERAL CONGENITAL AURAL ATRESIA
Authors: VANDERPOUW KTM SNIK AFM CREMERS CWRJ
Citation: Ktm. Vanderpouw et al., AUDIOMETRIC RESULTS OF BILATERAL BONE-ANCHORED HEARING-AID APPLICATION IN PATIENTS WITH BILATERAL CONGENITAL AURAL ATRESIA, The Laryngoscope, 108(4), 1998, pp. 548-553
BINAURAL APPLICATION OF THE BONE-ANCHORED HEARING-AID
Authors: SNIK AFM BEYNON AJ VANDERPOUW CTM MYLANUS EAM CREMERS CWRJ
Citation: Afm. Snik et al., BINAURAL APPLICATION OF THE BONE-ANCHORED HEARING-AID, The Annals of otology, rhinology & laryngology, 107(3), 1998, pp. 187-193
THE MOLECULAR-BASIS OF X-LINKED DEAFNESS TYPE-3 (DFN3) IN 2 SPORADIC CASES - IDENTIFICATION OF A SOMATIC MOSAICISM FOR A POU3F4 MISSENSE MUTATION
Authors: DEKOK YJM CREMERS CWRJ ROPERS HH CREMERS FPM
Citation: Yjm. Dekok et al., THE MOLECULAR-BASIS OF X-LINKED DEAFNESS TYPE-3 (DFN3) IN 2 SPORADIC CASES - IDENTIFICATION OF A SOMATIC MOSAICISM FOR A POU3F4 MISSENSE MUTATION, Human mutation, 10(3), 1997, pp. 207-211
LINKAGE ANALYSIS OF PROGRESSIVE HEARING-LOSS IN 5 EXTENDED FAMILIES MAPS THE DFNA1 GENE TO A 1.25-MB REGION ON CHROMOSOME 1P
Authors: VANCAMP G COUCKE PJ KUNST H SCHATTEMAN I VANVELZEN D MARRES H VANEWIJK M DECLAU F VANHAUWE P MEYERS J KENYON J SMITH SD SMITH RJH DJELANTIK B CREMERS CWRJ VANDEHEYNING PH WILLEMS PJ
Citation: G. Vancamp et al., LINKAGE ANALYSIS OF PROGRESSIVE HEARING-LOSS IN 5 EXTENDED FAMILIES MAPS THE DFNA1 GENE TO A 1.25-MB REGION ON CHROMOSOME 1P, Genomics, 41(1), 1997, pp. 70-74
THE GENE FOR PENDRED SYNDROME IS LOCATED BETWEEN D7S501 AND D7S692 INA 1.7-CM REGION ON CHROMOSOME 7Q
Authors: COUCKE P VANCAMP G DEMIRHAN O KABAKKAYA Y BALEMANS W VANHAUWE P VANAGTMAEL T SMITH RJH PARVING A BOLDER CHHM CREMERS CWRJ WILLEMS PJ
Citation: P. Coucke et al., THE GENE FOR PENDRED SYNDROME IS LOCATED BETWEEN D7S501 AND D7S692 INA 1.7-CM REGION ON CHROMOSOME 7Q, Genomics, 40(1), 1997, pp. 48-54
CONGENITAL CONDUCTIVE HEARING-LOSS IN THE LACRIMOAURICULODENTODIGITALSYNDROME
Authors: ENSINK RJH CREMERS CWRJ BRUNNER HG
Citation: Rjh. Ensink et al., CONGENITAL CONDUCTIVE HEARING-LOSS IN THE LACRIMOAURICULODENTODIGITALSYNDROME, Archives of otolaryngology, head & neck surgery, 123(1), 1997, pp. 97-99
GLOMUS TUMORS AND GENOMIC IMPRINTING - INFLUENCE OF INHERITANCE ALONGTHE PATERNAL OR MATERNAL LINE
Authors: STRUYCKEN PM CREMERS CWRJ MARIMAN ECM JOOSTEN FBM BLEKER RJTM
Citation: Pm. Struycken et al., GLOMUS TUMORS AND GENOMIC IMPRINTING - INFLUENCE OF INHERITANCE ALONGTHE PATERNAL OR MATERNAL LINE, Clinical otolaryngology and allied sciences, 22(1), 1997, pp. 71-76
HEARING-LOSS (IN NONOPERATED EARS) IN RELATION TO AGE IN OSTEOGENESISIMPERFECTA TYPE-I
Authors: GARRETSEN AJTM CREMERS CWRJ HUYGEN PLM
Citation: Ajtm. Garretsen et al., HEARING-LOSS (IN NONOPERATED EARS) IN RELATION TO AGE IN OSTEOGENESISIMPERFECTA TYPE-I, The Annals of otology, rhinology & laryngology, 106(7), 1997, pp. 575-582
Risultati: 1-25 | 26-50 | 51-75 | 76-81