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ANALYSIS OF A DEVELOPMENTAL GENE DELETED IN PATIENTS WITH WOLF-HIRSCHHORN-SYNDROME
Authors: STEC I DENDUNNEN JT WRIGHT TJ DEBOER PAJ VANHAERINGEN A MOORMAN AFM ALTHERR MR DONNAI D CROQUETTE MF TOUTAIN A VANOMMEN GJB
Citation: I. Stec et al., ANALYSIS OF A DEVELOPMENTAL GENE DELETED IN PATIENTS WITH WOLF-HIRSCHHORN-SYNDROME, European journal of human genetics, 6, 1998, pp. 6040-6040
WHSC1, A 90 KB SET DOMAIN-CONTAINING GENE, EXPRESSED IN EARLY DEVELOPMENT AND HOMOLOGOUS TO THE DROSOPHILA DYSMORPHY GENE MAPS IN THE WOLF-HIRSCHHORN-SYNDROME CRITICAL REGION AND IS FUSED TO IGH IN T(4-14) MULTIPLE-MYELOMA (VOL 7, PG 1071, 1998)
Authors: STEC I WRIGHT TJ VANOMMEN CJB DEBOER PAJ VANHAERINGEN A MOORMAN AFM ALTHERR MR DENDUNNEN JT
Citation: I. Stec et al., WHSC1, A 90 KB SET DOMAIN-CONTAINING GENE, EXPRESSED IN EARLY DEVELOPMENT AND HOMOLOGOUS TO THE DROSOPHILA DYSMORPHY GENE MAPS IN THE WOLF-HIRSCHHORN-SYNDROME CRITICAL REGION AND IS FUSED TO IGH IN T(4-14) MULTIPLE-MYELOMA (VOL 7, PG 1071, 1998), Human molecular genetics (Print), 7(9), 1998, pp. 1527-1528
WHSC1, A 90 KB SET DOMAIN-CONTAINING GENE, EXPRESSED IN EARLY DEVELOPMENT AND HOMOLOGOUS TO A DROSOPHILA DYSMORPHY GENE MAPS IN THE WOLF-HIRSCHHORN-SYNDROME CRITICAL REGION AND IS FUSED TO IGH IN T(4-14) MULTIPLE-MYELOMA
Authors: STEC I WRIGHT TJ VANOMMEN GJB DEBOER PAJ VANHAERINGEN A MOORMAN AFM ALTHERR MR DENDUNNEN JT
Citation: I. Stec et al., WHSC1, A 90 KB SET DOMAIN-CONTAINING GENE, EXPRESSED IN EARLY DEVELOPMENT AND HOMOLOGOUS TO A DROSOPHILA DYSMORPHY GENE MAPS IN THE WOLF-HIRSCHHORN-SYNDROME CRITICAL REGION AND IS FUSED TO IGH IN T(4-14) MULTIPLE-MYELOMA, Human molecular genetics (Print), 7(7), 1998, pp. 1071-1082
FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS)
Authors: DENDUNNEN JT KRAAYENBRINK T VANSCHOONEVELD M VANDEVOSSE E DEJONG PTVM TENBRINK JB SCHUURMAN E TIJMES N VANOMMEN GJB BERGEN AAB ANDOLFI G MONTINI E LI Y OUDET C BOLZ H KAPLAN J ORTH U GAL A HANAUER A BARDELLI AM AYUSO C DIAZ FJ BITOUN P VENTRUTO V BALLABIO A FRANCO B HIRIYANNA KT BINGHAM EL MCHENRY C PAWAR H COATS C DARGA T RICHARDS JE SIEVING PA HUOPANIEMI L RANTALA A ROSENBERG T DAHL N WRIGHT A DELACHAPELLE A ALITALO T LENZNER S BRUNNER B FEIL S NIESLER B SCHULZ U PINCKERS A BLANKENNAGEL A RUETHER K KELLNER U RAPPOLD G ROPERS HH KALSCHEUER V BERGER W TRUMP D WALPOLE SM NICOLAOU A GAYTHOR SA PIMENIDES D GEORGE NDL MOORE UT YATES JRW
Citation: Jt. Dendunnen et al., FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS), Human molecular genetics (Print), 7(7), 1998, pp. 1185-1192
CLINICAL-DIAGNOSIS OF HETEROZYGOUS DYSTROPHIN GENE DELETIONS BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: ROSENBERG C NAVAJAS L VAGENAS DF BAKKER E VAINZOF M PASSOSBUENO MR TAKATA RI VANOMMEN GJB ZATZ M DENDUNNEN JT
Citation: C. Rosenberg et al., CLINICAL-DIAGNOSIS OF HETEROZYGOUS DYSTROPHIN GENE DELETIONS BY FLUORESCENCE IN-SITU HYBRIDIZATION, Neuromuscular disorders, 8(7), 1998, pp. 447-452
CHARACTERIZATION OF SCML1, A NEW GENE IN XP22, WITH HOMOLOGY TO DEVELOPMENTAL POLYCOMB GENES
Authors: VANDEVOSSE E WALPOLE SM NICOLAOU A VANDERBENT P CAHN A VAUDIN M ROSS MT DURHAM J PAVITT R WILKINSON J GRAFHAM D BERGEN AAB VANOMMEN GJB YATES JRW DENDUNNEN JT TRUMP D
Citation: E. Vandevosse et al., CHARACTERIZATION OF SCML1, A NEW GENE IN XP22, WITH HOMOLOGY TO DEVELOPMENTAL POLYCOMB GENES, Genomics, 49(1), 1998, pp. 96-102
CENTROMERIC AND NONCENTROMERIC ADE2-SELECTABLE FRAGMENTATION VECTORS FOR YEAST ARTIFICIAL CHROMOSOMES IN AB1380
Authors: HEUS JJ DEWINTHER MPJ VANDEVOSSE E VANOMMEN GJB DENDUNNEN JT
Citation: Jj. Heus et al., CENTROMERIC AND NONCENTROMERIC ADE2-SELECTABLE FRAGMENTATION VECTORS FOR YEAST ARTIFICIAL CHROMOSOMES IN AB1380, PCR methods and applications, 7(6), 1997, pp. 657-660
A NOVEL HUMAN SERINE-THREONINE PHOSPHATASE RELATED TO THE DROSOPHILA RETINAL-DEGENERATION-C (RDGC) GENE IS SELECTIVELY EXPRESSED IN SENSORYNEURONS OF NEURAL CREST ORIGIN
Authors: MONTINI E RUGARLI EI VANDEVOSSE E ANDOLFI G MARIANI M PUCA AA CONSALEZ GG DENDUNNEN JT BALLABIO A FRANCO B
Citation: E. Montini et al., A NOVEL HUMAN SERINE-THREONINE PHOSPHATASE RELATED TO THE DROSOPHILA RETINAL-DEGENERATION-C (RDGC) GENE IS SELECTIVELY EXPRESSED IN SENSORYNEURONS OF NEURAL CREST ORIGIN, Human molecular genetics, 6(7), 1997, pp. 1137-1145
HIGH-RESOLUTION MAPPING BY YAC FRAGMENTATION OF A 2.5-MB XP22 REGION CONTAINING THE HUMAN RS, KFSD AND CLS DISEASE GENES
Authors: VANDEVOSSE E VANDERBENT P HEUS JJ VANOMMEN GJB DENDUNNEN JT
Citation: E. Vandevosse et al., HIGH-RESOLUTION MAPPING BY YAC FRAGMENTATION OF A 2.5-MB XP22 REGION CONTAINING THE HUMAN RS, KFSD AND CLS DISEASE GENES, Mammalian genome, 8(7), 1997, pp. 497-501
EXCLUSION OF PPEF AS THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS
Authors: VANDEVOSSE E FRANCO B VANDERBENT P MONTINI E ORTH U HANAUER A TIJMES N VANOMMEN GJB BALLABIO A DENDUNNEN JT BERGEN AAB
Citation: E. Vandevosse et al., EXCLUSION OF PPEF AS THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS, Human genetics, 101(2), 1997, pp. 235-237
A CANDIDATE GENE FOR X-LINKED RETINOSCHISIS IN XP22
Authors: TRUMP D WALPOLE SM VANDEVOSSE E NICOLAOU A CAHN A VAUDIN M ROSS MT DENDUNNEN JT YATES JRW
Citation: D. Trump et al., A CANDIDATE GENE FOR X-LINKED RETINOSCHISIS IN XP22, Journal of Medical Genetics, 34, 1997, pp. 18-18
A GENOME-SEQUENCE BASED APPROACH TO COMPUTATIONAL AND EXPERIMENTAL CANDIDATE GENE ANALYSIS OF WOLF-HIRSCHHORN-SYNDROME
Authors: STEC I DENDUNNEN JT VANHAERINGEN A CROQUETTE MF DONNAI D TOUTAIN A MOORMAN AFM DEBOER PAJ VANOMMEN GJB
Citation: I. Stec et al., A GENOME-SEQUENCE BASED APPROACH TO COMPUTATIONAL AND EXPERIMENTAL CANDIDATE GENE ANALYSIS OF WOLF-HIRSCHHORN-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1415-1415
IDENTIFICATION OF A CANDIDATE GENE FOR X-LINKED RETINOSCHISIS IN XP22
Authors: TRUMP D WALPOLE SM VANDEVOSSE E NICOLAOU A CAHN A VAUDIN M ROSS MT DENDUNNEN JT YATES JRW
Citation: D. Trump et al., IDENTIFICATION OF A CANDIDATE GENE FOR X-LINKED RETINOSCHISIS IN XP22, American journal of human genetics, 61(4), 1997, pp. 1427-1427
REFINEMENT OF THE LOCALIZATION OF THE X-LINKED RETINOSCHISIS GENE
Authors: BERGEN AAB VANDEVOSSE E FRANCO B VANDERBENT P BAKKER E MONTINI E HANAUER A TIJMES E VANOMMEN GJB BALLABIO A DENDUNNEN JT
Citation: Aab. Bergen et al., REFINEMENT OF THE LOCALIZATION OF THE X-LINKED RETINOSCHISIS GENE, American journal of human genetics, 61(4), 1997, pp. 1559-1559
ANALYSIS OF C-ELEGANS NEMATODES TRANSGENIC FOR THE START OF THE HD GENE WITH AND WITHOUT AN EXTENDED CAG-REPEAT
Authors: SMOOR MA DORSMAN JC BOUT M VANLUENEN HGAM PLASTERK RHA DENDUNNEN JT VANOMMEN GJB
Citation: Ma. Smoor et al., ANALYSIS OF C-ELEGANS NEMATODES TRANSGENIC FOR THE START OF THE HD GENE WITH AND WITHOUT AN EXTENDED CAG-REPEAT, American journal of human genetics, 61(4), 1997, pp. 1878-1878
THE DUCHENNE BECKER-MUSCULAR-DYSTROPHY DATA PAGES/
Authors: DENDUNNEN JT VANOMMEN GJB BAKKER E
Citation: Jt. Dendunnen et al., THE DUCHENNE BECKER-MUSCULAR-DYSTROPHY DATA PAGES/, American journal of human genetics, 61(4), 1997, pp. 2397-2397
AN XP22.1-P22.2 YAC CONTIG ENCOMPASSING THE DISEASE LOCI FOR RS, KFSD, CLS, HYP AND RP15 - REFINED LOCALIZATION OF RS
Authors: VANDEVOSSE E BERGEN AAB MEERSHOEK EJ OOSTERWIJK JC GREGORY S BAKKER B WEISSENBACH J COFFEY AJ VANOMMEN GJB DENDUNNEN JT
Citation: E. Vandevosse et al., AN XP22.1-P22.2 YAC CONTIG ENCOMPASSING THE DISEASE LOCI FOR RS, KFSD, CLS, HYP AND RP15 - REFINED LOCALIZATION OF RS, European journal of human genetics, 4(2), 1996, pp. 101-104
IDENTIFICATION OF A HOT-SPOT FOR MICRODELETIONS IN PATIENTS WITH X-LINKED DEAFNESS TYPE-3 (DFN3) 900 KB PROXIMAL TO THE DFN3 GENE POU3F4
Authors: DEKOK YJM VOSSENAAR ER CREMERS CWRJ DAHL N LAPORTE J HU LJ LACOMBE D FISCHELGHODSIAN N FRIEDMAN RA PARNES LS THORPE P BITNERGLINDZICZ M PANDER HJ HEILBRONNER H GRAVELINE J DENDUNNEN JT BRUNNER HG ROPERS HH CREMERS FPM
Citation: Yjm. Dekok et al., IDENTIFICATION OF A HOT-SPOT FOR MICRODELETIONS IN PATIENTS WITH X-LINKED DEAFNESS TYPE-3 (DFN3) 900 KB PROXIMAL TO THE DFN3 GENE POU3F4, Human molecular genetics, 5(9), 1996, pp. 1229-1235
SUBCELLULAR-LOCALIZATION OF THE HUNTINGTONS-DISEASE GENE-PRODUCT IN CELL-LINES BY IMMUNOFLUORESCENCE AND BIOCHEMICAL SUBCELLULAR FRACTIONATION
Authors: DEROOIJ KE DORSMAN JC SMOOR MA DENDUNNEN JT VANOMMEN GJB
Citation: Ke. Derooij et al., SUBCELLULAR-LOCALIZATION OF THE HUNTINGTONS-DISEASE GENE-PRODUCT IN CELL-LINES BY IMMUNOFLUORESCENCE AND BIOCHEMICAL SUBCELLULAR FRACTIONATION, Human molecular genetics, 5(8), 1996, pp. 1093-1099
APPLICATION OF IN-VITRO MYO-DIFFERENTIATION OF NONMUSCLE CELLS TO ENHANCE GENE-EXPRESSION AND FACILITATE ANALYSIS OF MUSCLE PROTEINS
Authors: ROEST PAM VANDERTUIJN AC GINJAAR HB HOEBEN RC HOGERVORST FBL BAKKER E DENDUNNEN JT VANOMMEN GJB
Citation: Pam. Roest et al., APPLICATION OF IN-VITRO MYO-DIFFERENTIATION OF NONMUSCLE CELLS TO ENHANCE GENE-EXPRESSION AND FACILITATE ANALYSIS OF MUSCLE PROTEINS, Neuromuscular disorders, 6(3), 1996, pp. 195-202
EXON MAPPING BY FIBER-FISH OR LR-PCR
Authors: FLORIJN RJ VANDERIJKE FM VROLIJK H BLONDEN LAJ HOFKER MH DENDUNNEN JT TANKE HJ VANOMMEN GJB RAAP AK
Citation: Rj. Florijn et al., EXON MAPPING BY FIBER-FISH OR LR-PCR, Genomics, 38(3), 1996, pp. 277-282
SCANNING FOR GENES IN LARGE GENOMIC REGIONS - COSMID-BASED EXON TRAPPING OF MULTIPLE EXONS IN A SINGLE-PRODUCT
Authors: DATSON NA VANDEVOSSE E DAUWERSE HG BOUT M VANOMMEN GJB DENDUNNEN JT
Citation: Na. Datson et al., SCANNING FOR GENES IN LARGE GENOMIC REGIONS - COSMID-BASED EXON TRAPPING OF MULTIPLE EXONS IN A SINGLE-PRODUCT, Nucleic acids research, 24(6), 1996, pp. 1105-1111
SPLICING MUTATIONS IN DMD BMD DETECTED BY RT-PCR/PTT - DETECTION OF A19AA INSERTION IN THE CYSTEINE-RICH DOMAIN OF DYSTROPHIN COMPATIBLE WITH BMD/
Authors: ROEST PAM BOUT M VANDERTUIJN AC GINJAAR IB BAKKER E HOGERVORST FBL VANOMMEN GJB DENDUNNEN JT
Citation: Pam. Roest et al., SPLICING MUTATIONS IN DMD BMD DETECTED BY RT-PCR/PTT - DETECTION OF A19AA INSERTION IN THE CYSTEINE-RICH DOMAIN OF DYSTROPHIN COMPATIBLE WITH BMD/, Journal of Medical Genetics, 33(11), 1996, pp. 935-939
CLOSING IN ON THE RIEGER SYNDROME GENE ON 4Q25 - MAPPING TRANSLOCATION BREAKPOINTS WITHIN A 50-KB REGION
Authors: DATSON NA SEMINA E VANSTAALDUINEN AAA DAUWERSE HG MEERSHOEK EJ HEUS JJ FRANTS RR DENDUNNEN JT MURRAY JC VANOMMEN GJB
Citation: Na. Datson et al., CLOSING IN ON THE RIEGER SYNDROME GENE ON 4Q25 - MAPPING TRANSLOCATION BREAKPOINTS WITHIN A 50-KB REGION, American journal of human genetics, 59(6), 1996, pp. 1297-1305
APPARENT GENE CONVERSIONS INVOLVING THE SMN GENE IN THE REGION OF THESPINAL MUSCULAR-ATROPHY LOCUS ON CHROMOSOME-5
Authors: VANDERSTEEGE G GROOTSCHOLTEN PM COBBEN JM ZAPPATA S SCHEFFER H DENDUNNEN JT VANOMMEN GJB BRAHE C BUYS CHCM
Citation: G. Vandersteege et al., APPARENT GENE CONVERSIONS INVOLVING THE SMN GENE IN THE REGION OF THESPINAL MUSCULAR-ATROPHY LOCUS ON CHROMOSOME-5, American journal of human genetics, 59(4), 1996, pp. 834-838
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