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1. Fodde, R; Kuipers, J; Rosenberg, C; Smits, R; Kielman, M; Gaspar, C; van Es, JH; Bruekel, C; Wiegant, J; Giles, RH; Clevers, H
   Mutations in the APC tumour suppressor gene cause chromosomal instability
   NATURE CELL BIOLOGY
   
   R. Fodde et al., "Mutations in the APC tumour suppressor gene cause chromosomal instability", NAT CELL BI, 3(4), 2001, pp. 433-438
2. Eriksson, L; Mertens, F; Akerman, M; Wiegant, J
   Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: Diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years
   JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
   
   L. Eriksson et al., "Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: Diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years", J ORAL MAX, 59(10), 2001, pp. 1217-1220
3. Gilhuis, HJ; Bernsen, HJJA; Jeuken, JWM; Wesseling, P; Sprenger, SHE; Kerstens, HMJ; Wiegant, J; Boerman, RH
   The relationship between genetic aberrations as detected by comparative genomic hybridization and vascularization in glioblastoma xenografts (vol 51,pg 121, 2001)
   JOURNAL OF NEURO-ONCOLOGY
   
   H.J. Gilhuis et al., "The relationship between genetic aberrations as detected by comparative genomic hybridization and vascularization in glioblastoma xenografts (vol 51,pg 121, 2001)", J NEURO-ONC, 53(1), 2001, pp. 77-78
4. Wiegant, J; Bezrookove, V; Rosenberg, C; Tanke, HJ; Raap, AK; Zhang, HG; Bittner, M; Trent, JM; Meltzer, P
   Differentially painting human chromosome arms with combined binary ratio-labeling fluorescence in situ hybridization
   GENOME RESEARCH
   
   J. Wiegant et al., "Differentially painting human chromosome arms with combined binary ratio-labeling fluorescence in situ hybridization", GENOME RES, 10(6), 2000, pp. 861-865
5. Szuhai, K; Bezrookove, V; Wiegant, J; Vrolijk, J; Dirks, RW; Rosenberg, C; Raap, AK; Tanke, HJ
   Simultaneous molecular karyotyping and mapping of viral DNA integration sites by 25-color COBRA-FISH
   GENES CHROMOSOMES & CANCER
   
   K. Szuhai et al., "Simultaneous molecular karyotyping and mapping of viral DNA integration sites by 25-color COBRA-FISH", GENE CHROM, 28(1), 2000, pp. 92-97
6. van Gijlswijk, RPM; van de Corput, MPC; Bezrookove, V; Wiegant, J; Tanke, HJ; Raap, AK
   Synthesis and purification of horseradish peroxidase-labeled oligonucleotides for tyramide-based fluorescence in situ hybridization
   HISTOCHEMISTRY AND CELL BIOLOGY
   
   R.P.M. van Gijlswijk et al., "Synthesis and purification of horseradish peroxidase-labeled oligonucleotides for tyramide-based fluorescence in situ hybridization", HISTOCHEM C, 113(3), 2000, pp. 175-180
7. Bezrookove, V; Hansson, K; van der Burg, M; van der Smagt, JJ; Hilhorst-Hofstee, Y; Wiegant, J; Beverstock, GC; Raap, AK; Tanke, H; Breuning, MH; Rosenberg, C
   Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH
   HUMAN GENETICS
   
   V. Bezrookove et al., "Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH", HUM GENET, 106(4), 2000, pp. 392-398
8. Gisselsson, D; Pettersson, L; Hoglund, M; Heidenblad, M; Gorunova, L; Wiegant, J; Mertens, F; Dal Cin, P; Mitelman, F; Mandahl, N
   Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
   
   D. Gisselsson et al., "Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity", P NAS US, 97(10), 2000, pp. 5357-5362
9. Tanke, HJ; Wiegant, J; van Gijlswijk, RPM; Bezrookove, V; Pattenier, H; Heetebrij, RJ; Talman, EG; Raap, AK; Vrolijk, J
   New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling
   EUROPEAN JOURNAL OF HUMAN GENETICS
   
   H.J. Tanke et al., "New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling", EUR J HUM G, 7(1), 1999, pp. 2-11
10. ROSENBERG C; VANGILSWIJK RPM; VOS CBJ; WIEGANT J; CORNELISSE CJ; TANKE HJ; RAAP AK
    COMPARATIVE GENOMIC HYBRIDIZATION WITH LISSAMINE-LABELED AND FLUORESCEIN-LABELED NUCLEOTIDES
    Cytometry
    
    C. Rosenberg et al., "COMPARATIVE GENOMIC HYBRIDIZATION WITH LISSAMINE-LABELED AND FLUORESCEIN-LABELED NUCLEOTIDES", Cytometry, 32(4), 1998, pp. 337-341
11. MIOZZO M; CASTORINA P; RIVA P; DALPRA L; CONTI AMF; VOLPI L; HOE TS; KHOO A; WIEGANT J; ROSENBERG C; LARIZZA L
    CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME
    International journal of cancer
    
    M. Miozzo et al., "CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME", International journal of cancer, 77(4), 1998, pp. 504-510
12. VANDECORPUT MPC; DIRKS RW; WIEGANT WW; WIEGANT J; MUHLEGGER K; RAAP AK
    ESTRADIOL, A NEW HAPTEN FOR DETECTING NUCLEIC-ACID SEQUENCES BY FISH
    HISTOCHEMISTRY AND CELL BIOLOGY
    
    M.P.C. Vandecorput et al., "ESTRADIOL, A NEW HAPTEN FOR DETECTING NUCLEIC-ACID SEQUENCES BY FISH", HISTOCHEM C, 108(4-5), 1997, pp. 359-364
13. LASAN R; LETICA L; HITREC V; MUZINIC D; BEGOVIC D; WIEGANT J
    IDENTIFICATION OF 3 CASES OF CHROMOSOME REARRANGEMENTS BY FLUORESCENCE IN-SITU HYBRIDIZATION
    Cytogenetics and cell genetics
    
    R. Lasan et al., "IDENTIFICATION OF 3 CASES OF CHROMOSOME REARRANGEMENTS BY FLUORESCENCE IN-SITU HYBRIDIZATION", Cytogenetics and cell genetics, 77(1-2), 1997, pp. 30-30
14. CASTORINA P; MIOZZO M; RIVA P; CONTI AMF; WIEGANT J; ROSENBERG C; DALPRA L; VOLPI L; MAK JW; LARIZZA L
    HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)
    Cytogenetics and cell genetics
    
    P. Castorina et al., "HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)", Cytogenetics and cell genetics, 77(1-2), 1997, pp. 103-103
15. GARCIAISIDORO M; TABERNERO MD; GARCIA JL; NAJERA ML; HERNANDEZ JM; WIEGANT J; RAAP A; SANMIGUEL J; ORFAO A
    DETECTION OF THE MBCR ABL TRANSLOCATION IN CHRONIC MYELOID-LEUKEMIA BY FLUORESCENCE IN-SITU HYBRIDIZATION - COMPARISON WITH CONVENTIONAL CYTOGENETICS AND IMPLICATIONS FOR MINIMAL RESIDUAL DISEASE DETECTION/
    Human pathology
    
    M. Garciaisidoro et al., "DETECTION OF THE MBCR ABL TRANSLOCATION IN CHRONIC MYELOID-LEUKEMIA BY FLUORESCENCE IN-SITU HYBRIDIZATION - COMPARISON WITH CONVENTIONAL CYTOGENETICS AND IMPLICATIONS FOR MINIMAL RESIDUAL DISEASE DETECTION/", Human pathology, 28(2), 1997, pp. 154-159
16. VANGIJLSWIJK RPM; ZIJLMANS HJMAA; WIEGANT J; BOBROW MN; ERICKSON TJ; ADLER KE; TANKE HJ; RAAP AK
    FLUOROCHROME-LABELED TYRAMIDES - USE IN IMMUNOCYTOCHEMISTRY AND FLUORESCENCE IN-SITU HYBRIDIZATION
    The Journal of histochemistry and cytochemistry
    
    R.P.M. Vangijlswijk et al., "FLUOROCHROME-LABELED TYRAMIDES - USE IN IMMUNOCYTOCHEMISTRY AND FLUORESCENCE IN-SITU HYBRIDIZATION", The Journal of histochemistry and cytochemistry, 45(3), 1997, pp. 375-382
17. FRANSZ PF; STAM M; MONTIJN B; TENHOOPEN R; WIEGANT J; KOOTER JM; OUD O; NANNINGA N
    DETECTION OF SINGLE-COPY GENES AND CHROMOSOME REARRANGEMENTS IN PETUNIA-HYBRIDA BY FLUORESCENCE IN-SITU HYBRIDIZATION
    Plant journal
    
    P.F. Fransz et al., "DETECTION OF SINGLE-COPY GENES AND CHROMOSOME REARRANGEMENTS IN PETUNIA-HYBRIDA BY FLUORESCENCE IN-SITU HYBRIDIZATION", Plant journal, 9(5), 1996, pp. 767-774
18. VANGIJLSWIJK RPM; WIEGANT J; VERVENNE R; LASAN R; TANKE HJ; RAAP AK
    HORSERADISH PEROXIDASE-LABELED OLIGONUCLEOTIDES AND FLUORESCENT TYRAMIDES FOR RAPID DETECTION OF CHROMOSOME-SPECIFIC REPEAT SEQUENCES
    Cytogenetics and cell genetics
    
    R.P.M. Vangijlswijk et al., "HORSERADISH PEROXIDASE-LABELED OLIGONUCLEOTIDES AND FLUORESCENT TYRAMIDES FOR RAPID DETECTION OF CHROMOSOME-SPECIFIC REPEAT SEQUENCES", Cytogenetics and cell genetics, 75(4), 1996, pp. 258-262
19. WIEGANT J; VERWOERD N; MASCHERETTI S; BOLK M; TANKE HJ; RAAP AK
    AN EVALUATION OF A NEW SERIES OF FLUORESCENT DUTPS FOR FLUORESCENCE IN-SITU HYBRIDIZATION
    The Journal of histochemistry and cytochemistry
    
    J. Wiegant et al., "AN EVALUATION OF A NEW SERIES OF FLUORESCENT DUTPS FOR FLUORESCENCE IN-SITU HYBRIDIZATION", The Journal of histochemistry and cytochemistry, 44(5), 1996, pp. 525-529
20. VANGIJLSWIJK RPM; WIEGANT J; RAAP AK; TANKE HJ
    IMPROVED LOCALIZATION OF FLUORESCENT TYRAMIDES FOR FLUORESCENCE IN-SITU HYBRIDIZATION USING DEXTRAN SULFATE AND POLYVINYL-ALCOHOL
    The Journal of histochemistry and cytochemistry
    
    R.P.M. Vangijlswijk et al., "IMPROVED LOCALIZATION OF FLUORESCENT TYRAMIDES FOR FLUORESCENCE IN-SITU HYBRIDIZATION USING DEXTRAN SULFATE AND POLYVINYL-ALCOHOL", The Journal of histochemistry and cytochemistry, 44(4), 1996, pp. 389-392
21. VANEIJSDEN R; JELSMA T; HEETEBRIJ R; BOELENS Y; WIEGANT J
    DEVELOPMENT OF A RAPID AND HIGHLY SENSITIVE LABELING METHOD OF DNA AND RNA PROBES FOR (FLUORESCENT) IN-SITU HYBRIDIZATION
    Clinical chemistry
    
    R. Vaneijsden et al., "DEVELOPMENT OF A RAPID AND HIGHLY SENSITIVE LABELING METHOD OF DNA AND RNA PROBES FOR (FLUORESCENT) IN-SITU HYBRIDIZATION", Clinical chemistry, 42(11), 1996, pp. 5-5
22. COIGNET LJA; SCHUURING E; KIBBELAAR RE; RAAP TK; KLEIVERDA KK; BERTHEAS MF; WIEGANT J; BEVERSTOCK G; KLUIN PM
    DETECTION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC NEOPLASIAS BY DOUBLE-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION
    Blood
    
    L.J.A. Coignet et al., "DETECTION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC NEOPLASIAS BY DOUBLE-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION", Blood, 87(4), 1996, pp. 1512-1519
23. TABERNERO D; SANMIGUEL JF; GARCIASANZ R; NAJERA L; GARCIAISIDORO M; PEREZSIMON JA; GONZALEZ M; WIEGANT J; RAAP AK; ORFAO A
    INCIDENCE OF CHROMOSOME NUMERICAL CHANGES IN MULTIPLE-MYELOMA - FLUORESCENCE IN-SITU HYBRIDIZATION ANALYSIS USING 15 CHROMOSOME-SPECIFIC PROBES
    The American journal of pathology
    
    D. Tabernero et al., "INCIDENCE OF CHROMOSOME NUMERICAL CHANGES IN MULTIPLE-MYELOMA - FLUORESCENCE IN-SITU HYBRIDIZATION ANALYSIS USING 15 CHROMOSOME-SPECIFIC PROBES", The American journal of pathology, 149(1), 1996, pp. 153-161
24. FLORIJN RJ; BONDEN LAJ; VROLIJK H; WIEGANT J; VAANDRAGER JW; BAAS F; DENDUNNEN JT; TANKE HJ; VANOMMEN GJB; RAAP AK
    HIGH-RESOLUTION DNA FIBER-FISH FOR GENOMIC DNA MAPPING AND COLOR BAR-CODING OF LARGE GENES
    Human molecular genetics
    
    R.J. Florijn et al., "HIGH-RESOLUTION DNA FIBER-FISH FOR GENOMIC DNA MAPPING AND COLOR BAR-CODING OF LARGE GENES", Human molecular genetics, 4(5), 1995, pp. 831-836
25. RAAP AK; VANDECORPUT MPC; VERVENNE RAW; VANGIJLSWIJK RPM; TANKE HJ; WIEGANT J
    ULTRA-SENSITIVE FISH USING PEROXIDASE-MEDIATED DEPOSITION OF BIOTIN-TYRAMIDE OR FLUOROCHROME-TYRAMIDE
    Human molecular genetics
    
    A.K. Raap et al., "ULTRA-SENSITIVE FISH USING PEROXIDASE-MEDIATED DEPOSITION OF BIOTIN-TYRAMIDE OR FLUOROCHROME-TYRAMIDE", Human molecular genetics, 4(4), 1995, pp. 529-534
26. TABERNERO MD; SANMIGUEL JF; GARCIA JL; GARCIAISIDORO M; WIEGANT J; CIUDAD J; GONZALEZ M; RIOS A; RAAP A; ORFAO A
    CLINICAL, BIOLOGICAL, AND IMMUNOPHENOTYPICAL CHARACTERISTICS OF B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA WITH TRISOMY-12 BY FLUORESCENCE IN-SITUHYBRIDIZATION
    Cytometry
    
    M.D. Tabernero et al., "CLINICAL, BIOLOGICAL, AND IMMUNOPHENOTYPICAL CHARACTERISTICS OF B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA WITH TRISOMY-12 BY FLUORESCENCE IN-SITUHYBRIDIZATION", Cytometry, 22(3), 1995, pp. 217-222
27. HOOVERS JMN; KALIKIN LM; JOHNSON LA; ALDERS M; REDEKER B; LAW DJ; BLIEK J; STEENMAN M; BENEDICT M; WIEGANT J; LENGAUER C; TAILLONMILLER P; SCHLESSINGER D; EDWARDS MC; ELLEDGE SJ; IVENS A; WESTERVELD A; LITTLE P; MANNENS M; FEINBERG AP
    MULTIPLE GENETIC-LOCI WITHIN 11P15 DEFINED BY BECKWITH-WIEDEMANN SYNDROME REARRANGEMENT BREAKPOINTS AND SUBCHROMOSOMAL TRANSFERABLE FRAGMENTS
    Proceedings of the National Academy of Sciences of the United Statesof America
    
    J.M.N. Hoovers et al., "MULTIPLE GENETIC-LOCI WITHIN 11P15 DEFINED BY BECKWITH-WIEDEMANN SYNDROME REARRANGEMENT BREAKPOINTS AND SUBCHROMOSOMAL TRANSFERABLE FRAGMENTS", Proceedings of the National Academy of Sciences of the United Statesof America, 92(26), 1995, pp. 12456-12460
28. TANKE HJ; FLORIJN RJ; WIEGANT J; RAAP AK; VROLIJK J
    CCD MICROSCOPY AND IMAGE-ANALYSIS OF CELLS AND CHROMOSOMES STAINED BYFLUORESCENCE IN-SITU HYBRIDIZATION
    Histochemical Journal
    
    H.J. Tanke et al., "CCD MICROSCOPY AND IMAGE-ANALYSIS OF CELLS AND CHROMOSOMES STAINED BYFLUORESCENCE IN-SITU HYBRIDIZATION", Histochemical Journal, 27(1), 1995, pp. 4-14
29. TABERNERO MD; ORFAO A; GARCIASANZ R; NAJERA ML; GARCIAISIDORO M; PEREZSIMON JA; GONZALEZ M; WIEGANT J; RAAP AK; SANMIGUEL JF
    CHROMOSOME NUMERICAL ABNORMALITIES IN MULTIPLE-MYELOMA ANALYZED BY FLUORESCENCE IN-SITU HYBRIDIZATION - A STUDY WITH 15 CHROMOSOME-SPECIFICPROBES
    Blood
    
    M.D. Tabernero et al., "CHROMOSOME NUMERICAL ABNORMALITIES IN MULTIPLE-MYELOMA ANALYZED BY FLUORESCENCE IN-SITU HYBRIDIZATION - A STUDY WITH 15 CHROMOSOME-SPECIFICPROBES", Blood, 86(10), 1995, pp. 226-226
30. COIGNET LJA; SCHUURING E; KIBBELAAR RE; RAAP AK; KLEIVERDA JK; BERTHEAS MF; WIEGANT J; BEVERSTOCK GC; KLUIN PM
    DELETION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC MALIGNANCIES BY DOUBLE COLOR FLUORESCENCE IN-SITU HYBRIDIZATION
    Blood
    
    L.J.A. Coignet et al., "DELETION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC MALIGNANCIES BY DOUBLE COLOR FLUORESCENCE IN-SITU HYBRIDIZATION", Blood, 86(10), 1995, pp. 1361-1361
31. DONEDA L; WIEGANT J; LARIZZA L
    3-WAY AND 2-WAY REARRANGEMENTS INVOLVING CHROMOSOMES 10, 2, 5 AND 5, 2 IN 2 MARKER CHROMOSOMES OF A HUMAN-MELANOMA CELL-LINE
    Melanoma research
    
    L. Doneda et al., "3-WAY AND 2-WAY REARRANGEMENTS INVOLVING CHROMOSOMES 10, 2, 5 AND 5, 2 IN 2 MARKER CHROMOSOMES OF A HUMAN-MELANOMA CELL-LINE", Melanoma research, 4(4), 1994, pp. 259-265
32. TAGARRO I; WIEGANT J; RAAP AK; GONZALEZAGUILERA JJ; FERNANDEZPERALTA AM
    ASSIGNMENT OF HUMAN SATELLITE-1 DNA AS REVEALED BY FLUORESCENT IN-SITU HYBRIDIZATION WITH OLIGONUCLEOTIDES
    Human genetics
    
    I. Tagarro et al., "ASSIGNMENT OF HUMAN SATELLITE-1 DNA AS REVEALED BY FLUORESCENT IN-SITU HYBRIDIZATION WITH OLIGONUCLEOTIDES", Human genetics, 93(2), 1994, pp. 125-128
33. HAGENAARS CE; KAWILARANGDEHAAS EWM; HAZEKAMP J; WIEGANT J; NIJWEIDE PJ
    OSTEOCLAST DEVELOPMENT IN THE COCULTURE SYSTEM OF PERIOSTLESS METATARSAL BONES AND HEMATOPOIETIC-CELLS STUDIED BY IN-SITU HYBRIDIZATION WITH A PROBE FOR Y-CHROMOSOMES
    Calcified tissue international
    
    C.E. Hagenaars et al., "OSTEOCLAST DEVELOPMENT IN THE COCULTURE SYSTEM OF PERIOSTLESS METATARSAL BONES AND HEMATOPOIETIC-CELLS STUDIED BY IN-SITU HYBRIDIZATION WITH A PROBE FOR Y-CHROMOSOMES", Calcified tissue international, 54(2), 1994, pp. 170-174
34. TABERNERO MD; GARCIA JL; GARCIAISIDORO M; WIEGANT J; RAAP A; GARCIAMARCOS MA; RIOS A; SANMIGUEL JF; ORFAO A
    CLINICAL, BIOLOGICAL AND IMMUNOPHENOTYPICAL CHARACTERISTICS OF B-CELLCHRONIC LYMPHOCYTIC-LEUKEMIA WITH TRISOMY-12 BY FLUORESCENCE IN-SITU HYBRIDIZATION
    Blood
    
    M.D. Tabernero et al., "CLINICAL, BIOLOGICAL AND IMMUNOPHENOTYPICAL CHARACTERISTICS OF B-CELLCHRONIC LYMPHOCYTIC-LEUKEMIA WITH TRISOMY-12 BY FLUORESCENCE IN-SITU HYBRIDIZATION", Blood, 84(10), 1994, pp. 10000460-10000460
35. ROELOFS H; SCHUURING E; WIEGANT J; MICHALIDES R; GIPHARTGASSLER M
    AMPLIFICATION OF THE 11Q13 REGION IN HUMAN CARCINOMA CELL-LINES - A MECHANISTIC VIEW
    Genes, chromosomes & cancer
    
    H. Roelofs et al., "AMPLIFICATION OF THE 11Q13 REGION IN HUMAN CARCINOMA CELL-LINES - A MECHANISTIC VIEW", Genes, chromosomes & cancer, 7(2), 1993, pp. 74-84
36. DAUWERSE JG; WESSELS JW; GILES RH; WIEGANT J; VANDERREIJDEN BA; FUGAZZA G; JUMELET EA; SMIT E; BAAS F; RAAP AK; HAGEMEIJER A; BEVERSTOCK GC; VANOMMEN GJB; BREUNING MH
    CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO
    Human molecular genetics
    
    J.G. Dauwerse et al., "CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO", Human molecular genetics, 2(10), 1993, pp. 1527-1534
37. ALKEMA MJ; WIEGANT J; RAAP AK; BERNS A; VANLOHUIZEN M
    CHARACTERIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PROTOONCOGENE BMI-1
    Human molecular genetics
    
    M.J. Alkema et al., "CHARACTERIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PROTOONCOGENE BMI-1", Human molecular genetics, 2(10), 1993, pp. 1597-1603
38. GIBBS S; FIJNEMAN R; WIEGANT J; VANKESSEL AG; VANDEPUTTE P; BACKENDORF C
    MOLECULAR CHARACTERIZATION AND EVOLUTION OF THE SPRR FAMILY OF KERATINOCYTE DIFFERENTIATION MARKERS ENCODING SMALL PROLINE-RICH PROTEINS
    Genomics
    
    S. Gibbs et al., "MOLECULAR CHARACTERIZATION AND EVOLUTION OF THE SPRR FAMILY OF KERATINOCYTE DIFFERENTIATION MARKERS ENCODING SMALL PROLINE-RICH PROTEINS", Genomics, 16(3), 1993, pp. 630-637
39. JONGMANS W; WIEGANT J; OSHIMURA M; JAMES MR; LOHMAN PHM; ZDZIENICKA MZ
    HUMAN CHROMOSOME-11 COMPLEMENTS ATAXIA-TELANGIECTASIA CELLS BUT DOES NOT COMPLEMENT THE DEFECT IN AT-LIKE CHINESE-HAMSTER CELL MUTANTS
    Human genetics
    
    W. Jongmans et al., "HUMAN CHROMOSOME-11 COMPLEMENTS ATAXIA-TELANGIECTASIA CELLS BUT DOES NOT COMPLEMENT THE DEFECT IN AT-LIKE CHINESE-HAMSTER CELL MUTANTS", Human genetics, 92(3), 1993, pp. 259-264
40. LEBO RV; CHANCE PF; DYCK PJ; REDILAFLORES MT; LYNCH ED; GOLBUS MS; BIRD TD; KING MC; ANDERSON LA; HALL J; WIEGANT J; JIANG ZR; DAZIN PF; PUNNETT HH; SCHONBERG SA; MOORE K; SHULL MM; GENDLER S; HURKO O; LOVELACE RE; LATOV N; TROFATTER J; CONNEALLY PM
    CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)
    Human genetics
    
    R.V. Lebo et al., "CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)", Human genetics, 91(3), 1993, pp. 301-301
41. SCHURINGBLOM GH; KEIJZER M; JAKOBS ME; VANDENBRANDE DM; VISSER HM; WIEGANT J; HOOVERS JMN; LESCHOT NJ
    MOLECULAR CYTOGENETIC ANALYSIS OF TERM PLACENTAE SUSPECTED OF MOSAICISM USING FLUORESCENCE IN-SITU HYBRIDIZATION
    Prenatal diagnosis
    
    G.H. Schuringblom et al., "MOLECULAR CYTOGENETIC ANALYSIS OF TERM PLACENTAE SUSPECTED OF MOSAICISM USING FLUORESCENCE IN-SITU HYBRIDIZATION", Prenatal diagnosis, 13(8), 1993, pp. 671-679
42. PUTMAN CAJ; DEGROOTH BG; WIEGANT J; RAAP AK; VANDERWERF KO; VANHULST NF; GREVE J
    DETECTION OF INSITU HYBRIDIZATION TO HUMAN-CHROMOSOMES WITH THE ATOMIC FORCE MICROSCOPE
    Cytometry
    
    C.A.J. Putman et al., "DETECTION OF INSITU HYBRIDIZATION TO HUMAN-CHROMOSOMES WITH THE ATOMIC FORCE MICROSCOPE", Cytometry, 14(4), 1993, pp. 356-361
43. MICHALOVA K; BARTSCH O; STARY J; JELINEK J; WIEGANT J; BUBANSKA E
    PARTIAL TRISOMY OF 3Q DETECTED BY CHROMOSOME PAINTING IN A CASE OF JUVENILE CHRONIC MYELOMONOCYTIC LEUKEMIA
    Cancer genetics and cytogenetics
    
    K. Michalova et al., "PARTIAL TRISOMY OF 3Q DETECTED BY CHROMOSOME PAINTING IN A CASE OF JUVENILE CHRONIC MYELOMONOCYTIC LEUKEMIA", Cancer genetics and cytogenetics, 71(1), 1993, pp. 67-70
44. SACCONE S; DESARIO A; WIEGANT J; RAAP AK; DELLAVALLE G; BERNARDI G
    CORRELATIONS BETWEEN ISOCHORES AND CHROMOSOMAL BANDS IN THE HUMAN GENOME
    Proceedings of the National Academy of Sciences of the United Statesof America
    
    S. Saccone et al., "CORRELATIONS BETWEEN ISOCHORES AND CHROMOSOMAL BANDS IN THE HUMAN GENOME", Proceedings of the National Academy of Sciences of the United Statesof America, 90(24), 1993, pp. 11929-11933
45. DAUWERSE JG; WESSELS JW; WIEGANT J; GILES RHG; HAGEMEIJER A; BAAS F; BEVERSTOCK G; VANOMMEN GJB; BREUNING MH
    CLONING THE REGION SPANNING THE INV(16) BREAKPOINT IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO
    American journal of human genetics
    
    J.G. Dauwerse et al., "CLONING THE REGION SPANNING THE INV(16) BREAKPOINT IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO", American journal of human genetics, 53(3), 1993, pp. 242-242