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Results: 1-8 |
Results: 8
MUTATIONS IN THE HUMAN ALPHA-TECTORIN GENE CAUSE AUTOSOMAL-DOMINANT NON-SYNDROMIC HEARING IMPAIRMENT
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
NON-SYNDROMIC DEAFNESS DFNA12 IS CAUSED BY MUTATIONS IN ALPHA-TECTORIN
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
A MOROCCAN FAMILY WITH AUTOSOMAL RECESSIVE SENSORINEURAL HEARING-LOSSCAUSED BY A MUTATION IN THE GAP JUNCTION PROTEIN GENE CONNEXIN-26 (GJB2)
Authors: LENCH NJ MARKHAM AF MUELLER RF KELSELL DP SMITH RJH WILLEMS PJ SCHATTEMAN I CAPON H VANDEHEYNING PJ VANCAMP G
Citation: Nj. Lench et al., A MOROCCAN FAMILY WITH AUTOSOMAL RECESSIVE SENSORINEURAL HEARING-LOSSCAUSED BY A MUTATION IN THE GAP JUNCTION PROTEIN GENE CONNEXIN-26 (GJB2), Journal of Medical Genetics, 35(2), 1998, pp. 151-152
REFINED MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS (DFNA5) TO A 2-CM REGION, AND EXCLUSION OF A CANDIDATE GENE THAT IS EXPRESSED IN THE COCHLEA
Authors: VANLAER L VANCAMP G VANZUIJLEN D GREEN ED VERSTREKEN M SCHATTEMAN I VANDEHEYNING P BALEMANS W COUCKE P GREINWALD JH SMITH RJH HUIZING E WILLEMS P
Citation: L. Vanlaer et al., REFINED MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS (DFNA5) TO A 2-CM REGION, AND EXCLUSION OF A CANDIDATE GENE THAT IS EXPRESSED IN THE COCHLEA, European journal of human genetics, 5(6), 1997, pp. 397-405
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
REFINEMENT OF THE DFNA5 CANDIDATE REGION, CONSTRUCTION OF A YAC CONTIG, AND EXCLUSION OF A FETAL-COCHLEAR EXPRESSED CANDIDATE GENE
Authors: VANLAER L VANCAMP G VANZUIJLEN D GREEN ED VERSTREKEN M SCHATTEMAN I VANDEHEYNING P BALEMANS W COUCKE P GREINWALD JH SMITH RJH HUIZING E WILLEMS P
Citation: L. Vanlaer et al., REFINEMENT OF THE DFNA5 CANDIDATE REGION, CONSTRUCTION OF A YAC CONTIG, AND EXCLUSION OF A FETAL-COCHLEAR EXPRESSED CANDIDATE GENE, American journal of human genetics, 61(4), 1997, pp. 1743-1743
A GENE FOR AUTOSOMAL-DOMINANT NONSYNDROMIC HEARING-LOSS (DFNA12) MAPSTO CHROMOSOME 11Q22-24
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
SELECTIVE VESTIBULAR NEURECTOMY IN MENIERES-DISEASE - A REVIEW
Authors: VANDEHEYNING PH VERLOOY J SCHATTEMAN I WUYTS FL
Citation: Ph. Vandeheyning et al., SELECTIVE VESTIBULAR NEURECTOMY IN MENIERES-DISEASE - A REVIEW, Acta oto-laryngologica, 1997, pp. 58-66
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