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