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Results: 1-6 |
Results: 6

Authors: VERHOEVEN K VANLAER L KIRSCHHOFER K LEGAN PK HUGHES DC SCHATTEMAN I VERSTREKEN M VANHAUWE P COUCKE P CHEN A SMITH RJH SOMERS T OFFECIERS FE VANDEHEYNING P RICHARDSON GP WACHTLER F KIMBERLING WT WILLEMS PJ GOVAERTS PJ VANCAMP G
Citation: K. Verhoeven et al., MUTATIONS IN THE HUMAN ALPHA-TECTORIN GENE CAUSE AUTOSOMAL-DOMINANT NON-SYNDROMIC HEARING IMPAIRMENT, Nature genetics, 19(1), 1998, pp. 60-62

Authors: VERHOEVEN K VANLAER L KIRSCHHOFER K LEGAN K HUGHES D VERSTREKEN M GOVAERTS PJ SCHATTEMAN I VANHAUWE P SMITH RJH VANDEHEYNING P WACHTLER F KIMBERLING B WILLEMS PJ VANCAMP G
Citation: K. Verhoeven et al., NON-SYNDROMIC DEAFNESS DFNA12 IS CAUSED BY MUTATIONS IN ALPHA-TECTORIN, European journal of human genetics, 6, 1998, pp. 504-504

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

Authors: CHEN AH MUELLER RF PRASAD SD GREINWALD JH MANALIGOD J MUILENBURG AC VERHOEVEN K VANCAMP G SMITH RJH
Citation: Ah. Chen et al., PRESYMPTOMATIC DIAGNOSIS OF NONSYNDROMIC HEARING-LOSS BY GENOTYPING, Archives of otolaryngology, head & neck surgery, 124(1), 1998, pp. 20-24

Authors: SCOTT DA GREINWALD JH MARIETTA JR DRURY S SWIDERSKI RE VINAS A DEANGELIS MM CARMI R RAMESH A KRAFT ML SKWORAK AB FRIEDMAN RA SRISAILAPATHY CRS VERHOEVEN K VANCAMP G LOVETT M DEININGER PL BATZER MA MORTON CC KEATS BJ SMITH RJH SHEFFIELD VC
Citation: Da. Scott et al., IDENTIFICATION AND MUTATION ANALYSIS OF A COCHLEAR-EXPRESSED, ZINC-FINGER PROTEIN GENE AT THE DFNB7 11 AND DN HEARING-LOSS-LOCI ON HUMAN-CHROMOSOME 9Q AND MOUSE-CHROMOSOME-19/, Gene, 215(2), 1998, pp. 461-469

Authors: VERHOEVEN K VANCAMP G GOVAERTS PJ BALEMANS W SCHATTEMAN I VERSTREKEN M VANLAER L SMITH RJH BROWN MR VANDEHEYNING PH SOMERS T OFFECIERS FE WILLEMS PJ
Citation: K. Verhoeven et al., A GENE FOR AUTOSOMAL-DOMINANT NONSYNDROMIC HEARING-LOSS (DFNA12) MAPSTO CHROMOSOME 11Q22-24, American journal of human genetics, 60(5), 1997, pp. 1168-1173
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