Authors:
VANLAER L
HUIZING EH
VERSTREKEN M
VANZUIJLEN D
WAUTERS JG
BOSSUYT PJ
VANDEHEYNING P
MCGUIRT WT
SMITH RJH
WILLEMS PJ
LEGAN PK
RICHARDSON GP
VANCAMP G
Citation: L. Vanlaer et al., NONSYNDROMIC HEARING IMPAIRMENT IS ASSOCIATED WITH A MUTATION IN DFNA5, Nature genetics, 20(2), 1998, pp. 194-197
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:
VANHAUWE P
EVERETT L
COUCKE P
CHEN A
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BOLDER C
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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
Authors:
KOOY F
REYNIERS E
VERHOYE M
SIJBERS J
FRANSEN E
OOSTRA BA
WILLEMS PJ
VANDERLINDEN A
Citation: F. Kooy et al., MRI AS A TOOL TO STUDY BRAIN STRUCTURE FROM MOUSE MODELS OF MENTAL-RETARDATION, European journal of human genetics, 6, 1998, pp. 306-306
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:
FRANSEN E
DHOOGE R
KOOY RF
VANCAMP G
VANDERLINDEN A
DEDEYN P
WILLEMS PJ
Citation: E. Fransen et al., L1 KNOCKOUT MICE SHOW DILATED VENTRICLES, VERMIS HYPOPLASIA AND IMPAIRED EXPLORATION PATTERNS, European journal of human genetics, 6, 1998, pp. 1075-1075
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
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CREMERS CWRJ
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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
Authors:
FRANSEN E
DHOOGE R
VANCAMP G
VERHOYE M
SIJBERS J
REYNIERS E
SORIANO P
KAMIGUCHI H
WILLEMSEN R
KOEKKOEK SKE
DEZEEUW CI
DEDEYN PP
VANDERLINDEN A
LEMMON V
KOOY RF
WILLEMS PJ
Citation: E. Fransen et al., L1 KNOCKOUT MICE SHOW DILATED VENTRICLES, VERMIS HYPOPLASIA AND IMPAIRED EXPLORATION PATTERNS, Human molecular genetics, 7(6), 1998, pp. 999-1009
Citation: O. Steward et al., NO EVIDENCE FOR DISRUPTION OF NORMAL PATTERNS OF MESSENGER-RNA LOCALIZATION IN DENDRITES OR DENDRITIC TRANSPORT OF RECENTLY SYNTHESIZED MESSENGER-RNA IN FMR1 KNOCKOUT MICE, A MODEL FOR HUMAN FRAGILE-X MENTAL-RETARDATION SYNDROME, NeuroReport, 9(3), 1998, pp. 477-481
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:
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
Authors:
WUYTS W
VANHUL W
DEBOULLE K
HENDRICKX J
BAKKER E
VANHOENACKER F
MOLLICA F
LUDECKE HJ
SAYLI BS
PAZZAGLIA UE
MORTIER G
HAMEL B
CONRAD EU
MATSUSHITA M
RASKIND WH
WILLEMS PJ
Citation: W. Wuyts et al., MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES, American journal of human genetics, 62(2), 1998, pp. 346-354
Authors:
VANHUL W
BALEMANS W
VANHUL E
DIKKERS FG
OBEE H
STOKROOS RJ
HILDERING P
VANHOENACKER F
VANCAMP G
WILLEMS PJ
Citation: W. Vanhul et al., VAN-BUCHEM-DISEASE (HYPEROSTOSIS CORTICALIS GENERALISATA) MAPS TO CHROMOSOME 17Q12-Q21, American journal of human genetics, 62(2), 1998, pp. 391-399
Authors:
WUYTS W
VANHUL W
HENDRICKX J
SPELEMAN F
WAUTERS J
DEBOULLE K
VANROY N
VANAGTMAEL T
BOSSUYT P
WILLEMS PJ
Citation: W. Wuyts et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2, European journal of human genetics, 5(6), 1997, pp. 382-389
Authors:
BIDAUD C
SALOMON R
VANCAMP G
PELET A
ATTIE T
ENG C
BONDUELLE M
AMIEL J
NIHOULFEKETE C
WILLEMS PJ
MUNNICH A
LYONNET S
Citation: C. Bidaud et al., ENDOTHELIN-3 GENE-MUTATIONS IN ISOLATED AND SYNDROMIC HIRSCHSPRUNG-DISEASE, European journal of human genetics, 5(4), 1997, pp. 247-251
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
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
Authors:
VANHUL W
BOLLERSLEV J
GRAM J
VANHUL E
BENICHOU O
WILLEMS PJ
Citation: W. Vanhul et al., LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT OSTEOPETROSIS (ALBERS-SCHONBERG-DISEASE) TO CHROMOSOME 1P21, Journal of bone and mineral research, 12, 1997, pp. 660-660
Authors:
VANHUL W
WUYTS W
HENDRICKX J
WAUTERS J
DEBOULLE K
WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY, Journal of bone and mineral research, 12, 1997, pp. 661-661