Authors:
LEMMERS RJLF
VANDERMAAREL SM
VANDEUTEKOM JCT
VANDERWIELEN MJR
DEIDDA G
DAUWERSE HG
HEWITT J
HOFKER M
BAKKER E
PADBERG GW
FRANTS RR
Citation: Rjlf. Lemmers et al., INTERCHROMOSOMAL AND INTRACHROMOSOMAL SUB-TELOMERIC REARRANGEMENTS ON4Q35 - IMPLICATIONS FOR FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)ETIOLOGY AND DIAGNOSIS, Human molecular genetics (Print), 7(8), 1998, pp. 1207-1214
Authors:
VANDEUTEKOM JCT
FLOYD SS
BOOTH DK
OLIGINO T
KRISKY D
MARCONI P
GLORIOSO JC
HUARD J
Citation: Jct. Vandeutekom et al., IMPLICATIONS OF MATURATION FOR VIRAL GENE DELIVERY TO SKELETAL-MUSCLE, Neuromuscular disorders, 8(3-4), 1998, pp. 135-148
Authors:
QU ZQ
BALKIR L
VANDEUTEKOM JCT
ROBBINS PD
PRUCHNIC R
HUARD J
Citation: Zq. Qu et al., DEVELOPMENT OF APPROACHES TO IMPROVE CELL-SURVIVAL IN MYOBLAST TRANSFER THERAPY, The Journal of cell biology, 142(5), 1998, pp. 1257-1267
Authors:
GREWAL PK
VANDEUTEKOM JCT
MILLS KA
LEMMERS RJLF
MATHEWS KD
FRANTS RR
HEWITT JE
Citation: Pk. Grewal et al., THE MOUSE HOMOLOG OF FRG1, A CANDIDATE GENE FOR FSHD, MAPS PROXIMAL TO THE MYODYSTROPHY MUTATION ON CHROMOSOME-8, Mammalian genome, 8(6), 1997, pp. 394-398
Authors:
VANDERMAAREL SM
LEMMERS RJL
VANDEUTEKOM JCT
BAKKER E
VANDERWIELEN MJR
BIK E
HOFKER MH
PADBERG GW
FRANTS RR
Citation: Sm. Vandermaarel et al., MORE INSIGHT IN THE GENETIC MECHANISMS UNDERLYING FACIOSCAPULOHUMERALMUSCULAR-DYSTROPHY, American journal of human genetics, 61(4), 1997, pp. 277-277
Authors:
VANDEUTEKOM JCT
LEMMERS RJLF
GREWAL PK
VANGEEL M
ROMBERG S
DAUWERSE HG
WRIGHT TJ
PADBERG GW
HOFKER MH
HEWITT JE
FRANTS RR
Citation: Jct. Vandeutekom et al., IDENTIFICATION OF THE FIRST GENE (FRG1) FROM THE FSHD REGION ON HUMAN-CHROMOSOME 4Q35, Human molecular genetics, 5(5), 1996, pp. 581-590
Authors:
VANDEUTEKOM JCT
BAKKER E
LEMMERS RJLF
VANDERWIELEN MJR
BIK E
HOFKER MH
PADBERG GW
FRANTS RR
Citation: Jct. Vandeutekom et al., EVIDENCE FOR SUBTELOMERIC EXCHANGE OF 3.3 KB TANDEMLY REPEATED UNITS BETWEEN CHROMOSOMES 4Q35 AND 10Q26 - IMPLICATIONS FOR GENETIC-COUNSELING AND ETIOLOGY OF FSHD1, Human molecular genetics, 5(12), 1996, pp. 1997-2003
Authors:
VANDEUTEKOM JCT
HOFKER MH
ROMBERG S
VANGEEL M
ROMMENS J
WRIGHT TJ
HEWITT JE
PADBERG GW
WIJMENGA C
FRANTS RR
Citation: Jct. Vandeutekom et al., SEARCH FOR THE FSHD GENE USING CDNA SELECTION IN A REGION SPANNING 100-KB ON CHROMOSOME-4Q35, Muscle & nerve, 1995, pp. 19-26
Authors:
HAZAN J
FONTAINE B
BRUYN RPM
LAMY C
VANDEUTEKOM JCT
RIME CS
DURR A
MELKI J
LYONCAEN O
AGID Y
MUNNICH A
PADBERG GW
DERECONDO J
FRANTS RR
BRICE A
WEISSENBACH J
Citation: J. Hazan et al., LINKAGE OF A NEW LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME 2P, Human molecular genetics, 3(9), 1994, pp. 1569-1573
Authors:
HEWITT JE
LYLE R
CLARK LN
VALLELEY EM
WRIGHT TJ
WIJMENGA C
VANDEUTEKOM JCT
FRANCIS F
SHARPE PT
HOFKER M
FRANTS RR
WILLIAMSON R
Citation: Je. Hewitt et al., ANALYSIS OF THE TANDEM REPEAT LOCUS D4Z4 ASSOCIATED WITH FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, Human molecular genetics, 3(8), 1994, pp. 1287-1295
Authors:
WIJMENGA C
VANDEUTEKOM JCT
HEWITT JE
PADBERG GW
VANOMMEN GJB
HOFKER MH
FRANTS RR
Citation: C. Wijmenga et al., PULSED-FIELD GEL-ELECTROPHORESIS OF THE D4F104S1 LOCUS REVEALS THE SIZE AND THE PARENTAL ORIGIN OF THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD)-ASSOCIATED DELETIONS, Genomics, 19(1), 1994, pp. 21-26
Authors:
VANDEUTEKOM JCT
BRUYN RPM
VANDENBOORN N
SANDKUIJL LA
PADBERG GW
FRANTS RR
Citation: Jct. Vandeutekom et al., PURE HEREDITARY SPASTIC PARAPARESIS - AN EXCLUSION MAP COVERING MORE THAN 40-PERCENT OF THE AUTOSOMAL GENOME, Human genetics, 93(4), 1994, pp. 408-414
Authors:
VANDEUTEKOM JCT
WIJMENGA C
VANTIENHOVEN EAE
GRUTER AM
FRANTS RR
HEWITT JE
PADBERG GW
VANOMMEN GJB
HOFKER MH
Citation: Jct. Vandeutekom et al., FSHD ASSOCIATED DNA REARRANGEMENTS ARE DUE TO DELETIONS OF INTEGRAL COPIES OF A 3.2 KB TANDEMLY REPEATED UNIT, Human molecular genetics, 2(12), 1993, pp. 2037-2042
Authors:
FRANTS RR
VANDEUTEKOM JCT
ROMMENS J
HEWITT JE
DATSON NA
VANGEEL M
ROMBERG S
VANOMMEN GJB
PADBERG GW
HOFKER MH
WIJMENGA C
Citation: Rr. Frants et al., ISOLATION OF CDNAS FROM THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY REGION, American journal of human genetics, 53(3), 1993, pp. 54-54