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1. Santos, CB; Lima, MAC; Pimentel, MMG
   A new PCR assay useful for screening of FRAXE/FMR2 mental impairment amongmales
   HUMAN MUTATION
   
   C.B. Santos et al., "A new PCR assay useful for screening of FRAXE/FMR2 mental impairment amongmales", HUM MUTAT, 18(2), 2001, pp. 157-162
2. State, MW; Pauls, DL; Leckman, JF
   Tourette's syndrome and related disorders
   CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
   
   M.W. State et al., "Tourette's syndrome and related disorders", CH ADOLESC, 10(2), 2001, pp. 317
3. Andersen, MK; Christiansen, DH; Kirchhoff, M; Pedersen-Bjergaard, J
   Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents
   GENES CHROMOSOMES & CANCER
   
   M.K. Andersen et al., "Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents", GENE CHROM, 31(1), 2001, pp. 33-41
4. Padilla-Nash, HM; Heselmeyer-Haddad, K; Wangsa, N; Zhang, HG; Ghadimi, BM; Macville, M; Augustus, M; Schrock, E; Hilgenfeld, E; Ried, T
   Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms
   GENES CHROMOSOMES & CANCER
   
   H.M. Padilla-Nash et al., "Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms", GENE CHROM, 30(4), 2001, pp. 349-363
5. Fang, JM; Arlt, MF; Burgess, AC; Dagenais, SL; Beer, DG; Glover, TW
   Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome3 in an esophageal adenocarcinoma
   GENES CHROMOSOMES & CANCER
   
   J.M. Fang et al., "Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome3 in an esophageal adenocarcinoma", GENE CHROM, 30(3), 2001, pp. 292-298
6. Weinstein, SJ; Ziegler, RG; Selhub, J; Fears, TR; Strickler, HD; Brinton, LA; Hamman, RF; Levine, RS; Mallin, K; Stolley, PD
   Elevated serum homocysteine levels and increased risk of invasive cervicalcancer in US women
   CANCER CAUSES & CONTROL
   
   S.J. Weinstein et al., "Elevated serum homocysteine levels and increased risk of invasive cervicalcancer in US women", CANC CAUSE, 12(4), 2001, pp. 317-324
7. Michael, D; Rajewsky, MF
   Induction of the common fragile site FRA3B does not affect FHIT expression
   ONCOGENE
   
   D. Michael e M.F. Rajewsky, "Induction of the common fragile site FRA3B does not affect FHIT expression", ONCOGENE, 20(14), 2001, pp. 1798-1801
8. Perl, A
   Endogenous retroviruses in pathogenesis of autoimmunity
   JOURNAL OF RHEUMATOLOGY
   
   A. Perl, "Endogenous retroviruses in pathogenesis of autoimmunity", J RHEUMATOL, 28(3), 2001, pp. 461-464
9. Savelyeva, L; Schwab, M
   Amplification of oncogenes revisited: from expression profiling to clinical application
   CANCER LETTERS
   
   L. Savelyeva e M. Schwab, "Amplification of oncogenes revisited: from expression profiling to clinical application", CANCER LETT, 167(2), 2001, pp. 115-123
10. Bolivar, J; Garcia-Cozar, FJ; Astola, A; Iglesias, C; Pendon, C; Valdivia, MM
    Genomic structure and chromosome location of the human gene encoding the zinc finger autoantigen ZNF330
    CYTOGENETICS AND CELL GENETICS
    
    J. Bolivar et al., "Genomic structure and chromosome location of the human gene encoding the zinc finger autoantigen ZNF330", CYTOG C GEN, 93(3-4), 2001, pp. 234-238
11. Ray, GN; Shahid, M; Husain, SA
    Status of chromosome breaks and gaps in breast cancer: a follow-up study
    CANCER GENETICS AND CYTOGENETICS
    
    G.N. Ray et al., "Status of chromosome breaks and gaps in breast cancer: a follow-up study", CANC GENET, 130(2), 2001, pp. 155-159
12. Latham, C; Zhang, AJ; Nalbanti, A; Maner, S; Zickert, P; Blegen, H; Zetterberg, A
    Frequent co-amplification of two different regions on 17q in aneuploid breast carcinomas
    CANCER GENETICS AND CYTOGENETICS
    
    C. Latham et al., "Frequent co-amplification of two different regions on 17q in aneuploid breast carcinomas", CANC GENET, 127(1), 2001, pp. 16-23
13. Maluf, SW; Erdtmann, B
    Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis
    CANCER GENETICS AND CYTOGENETICS
    
    S.W. Maluf e B. Erdtmann, "Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis", CANC GENET, 124(1), 2001, pp. 71-75
14. Megarbane, A; Waked, N; Chouery, E; Moglabey, YB; Saliba, N; Mornet, E; Serre, JL; Slim, R
    Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    A. Megarbane et al., "Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers", AM J MED G, 98(3), 2001, pp. 244-249
15. Plaja, A; Miro, R; Fuster, C; Perez, C; Sarret, E; Esteve, P; Egozcue, J
    Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood cultures
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    A. Plaja et al., "Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood cultures", AM J MED G, 101(2), 2001, pp. 106-113
16. Odierna, G; Aprea, G; Arribas, O; Carriglione, T
    A chromosomal study of the Pyrenean endemic brown frog species, Rana pyrenaica, and various Italian populations of R-dalmatina and R-italica
    FOLIA ZOOLOGICA
    
    G. Odierna et al., "A chromosomal study of the Pyrenean endemic brown frog species, Rana pyrenaica, and various Italian populations of R-dalmatina and R-italica", FOL ZOOL, 50(1), 2001, pp. 55-63
17. Smith, L; Plug, A; Thayer, M
    Delayed replication timing leads to delayed mitotic chromosome condensation and chromosomal instability of chromosome translocations
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    L. Smith et al., "Delayed replication timing leads to delayed mitotic chromosome condensation and chromosomal instability of chromosome translocations", P NAS US, 98(23), 2001, pp. 13300-13305
18. Kolomietz, E; Al-Maghrabi, J; Brennan, S; Karaskova, J; Minkin, S; Lipton, J; Squire, JA
    Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
    BLOOD
    
    E. Kolomietz et al., "Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis", BLOOD, 97(11), 2001, pp. 3581-3588
19. Kannan, K; Munirajan, AK; Bhuvarahamurthy, V; Mohanprasad, BKC; Shankar, P; Tsuchida, N; Shanmugam, G
    FHIT Gene mutations and single nucleotide polymorphism in Indian oral and cervical squamous cell carcinomas
    ORAL ONCOLOGY
    
    K. Kannan et al., "FHIT Gene mutations and single nucleotide polymorphism in Indian oral and cervical squamous cell carcinomas", ORAL ONCOL, 36(2), 2000, pp. 189-193
20. Yamauchi, M; Tsuji, S; Mita, K; Saito, T; Morimyo, M
    A novel minisatellite repeat expansion identified at FRA16B in a Japanese carrier.
    GENES & GENETIC SYSTEMS
    
    M. Yamauchi et al., "A novel minisatellite repeat expansion identified at FRA16B in a Japanese carrier.", GENE GEN SY, 75(3), 2000, pp. 149-154
21. Karkera, JD; Ayache, S; Ransome, RJ; Jackson, MA; Elsayem, AF; Sridhar, R; Detera-Wadleigh, SD; Wadleigh, RG
    Refinement of regions with allelic loss on chromosome 18p11.2 and 18q12.2 in esophageal squamous cell carcinoma
    CLINICAL CANCER RESEARCH
    
    J.D. Karkera et al., "Refinement of regions with allelic loss on chromosome 18p11.2 and 18q12.2 in esophageal squamous cell carcinoma", CLIN CANC R, 6(9), 2000, pp. 3565-3569
22. 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
23. Egeli, U; Ozkan, L; Tunca, B; Kahraman, S; Cecener, G; Ergul, E; Engin, K
    The relationship between genetic susceptibility to head and neck cancer with the expression of common fragile sites
    HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
    
    U. Egeli et al., "The relationship between genetic susceptibility to head and neck cancer with the expression of common fragile sites", HEAD NECK, 22(6), 2000, pp. 591-598
24. Fundia, A; Gorostiaga, M; Mudry, M
    Expression of common fragile sites in two Ceboidea species: Saimiri boliviensis and Alouatta caraya (Primates : Platyrrhini)
    GENETICS SELECTION EVOLUTION
    
    A. Fundia et al., "Expression of common fragile sites in two Ceboidea species: Saimiri boliviensis and Alouatta caraya (Primates : Platyrrhini)", GEN SEL EVO, 32(1), 2000, pp. 87-97
25. Adra, CN; Donato, JL; Badovinac, R; Syed, F; Kheraj, R; Cai, HB; Moran, C; Kolker, MT; Turner, H; Weremowicz, S; Shirakawa, T; Morton, CC; Schnipper, LE; Drews, R
    SMARCAD1, a novel human helicase family-defining member associated with genetic instability: Cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases
    GENOMICS
    
    C.N. Adra et al., "SMARCAD1, a novel human helicase family-defining member associated with genetic instability: Cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases", GENOMICS, 69(2), 2000, pp. 162-173
26. Courtay-Cahen, C; Morris, JS; Edwards, PAW
    Chromosome translocations in breast cancer with breakpoints at 8p12
    GENOMICS
    
    C. Courtay-Cahen et al., "Chromosome translocations in breast cancer with breakpoints at 8p12", GENOMICS, 66(1), 2000, pp. 15-25
27. Lindquist, R; Forsblom, AM; Ost, A; Gahrton, G
    Mutagen exposures and chromosome 3 aberrations in acute myelocytic leukemia
    LEUKEMIA
    
    R. Lindquist et al., "Mutagen exposures and chromosome 3 aberrations in acute myelocytic leukemia", LEUKEMIA, 14(1), 2000, pp. 112-118
28. Bode, J; Benham, C; Ernst, E; Knopp, A; Marschalek, R; Strick, R; Strissel, P
    Fatal connections: When DNA ends meet on the nuclear matrix
    JOURNAL OF CELLULAR BIOCHEMISTRY
    
    J. Bode et al., "Fatal connections: When DNA ends meet on the nuclear matrix", J CELL BIOC, 2000, pp. 3-22
29. Tukun, A; Renda, Y; Topcu, M; Tuncali, T; Bokesoy, I
    Mental retardation with rare fragile site expressed at 2q11
    BRAIN & DEVELOPMENT
    
    A. Tukun et al., "Mental retardation with rare fragile site expressed at 2q11", BRAIN DEVEL, 22(8), 2000, pp. 498-500
30. Morelli, C; Magnanini, C; Mungall, AJ; Negrini, M; Barbanti-Brodano, G
    Cloning and characterization of two overlapping genes in a subregion at 6q21 involved in replicative senescence and schizophrenia
    GENE
    
    C. Morelli et al., "Cloning and characterization of two overlapping genes in a subregion at 6q21 involved in replicative senescence and schizophrenia", GENE, 252(1-2), 2000, pp. 217-225
31. Tunca, B; Egeli, U; Zorluoglu, A; Yilmazlar, T; Yerci, O; Kizil, A
    The expression of fragile sites in lymphocytes of patients with rectum cancer and their first-degree relatives
    CANCER LETTERS
    
    B. Tunca et al., "The expression of fragile sites in lymphocytes of patients with rectum cancer and their first-degree relatives", CANCER LETT, 152(2), 2000, pp. 201-209
32. Roy, SK; Trivedi, AH; Bakshi, SR; Patel, RK; Shukla, PH; Patel, SJ; Bhatavdekar, JM; Patel, DD; Shah, PM
    Spontaneous chromosomal instability in breast cancer families
    CANCER GENETICS AND CYTOGENETICS
    
    S.K. Roy et al., "Spontaneous chromosomal instability in breast cancer families", CANC GENET, 118(1), 2000, pp. 52-56
33. Thomson, SW; Heimburger, DC; Cornwell, PE; Turner, ME; Sauberlich, HE; Fox, LM; Butterworth, CE
    Effect of total plasma homocysteine on cervical dysplasia risk
    NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL
    
    S.W. Thomson et al., "Effect of total plasma homocysteine on cervical dysplasia risk", NUTR CANCER, 37(2), 2000, pp. 128-133
34. Kerbeshian, J; Severud, R; Burd, L; Larson, L
    Peek-a-boo fragile site at 16D associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    J. Kerbeshian et al., "Peek-a-boo fragile site at 16D associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation", AM J MED G, 96(1), 2000, pp. 69-73
35. Luceri, C; Guglielmi, F; De Filippo, C; Caderni, G; Mini, E; Biggeri, A; Napoli, C; Tonelli, F; Cianchi, F; Dolara, P
    Clinicopathologic features and FHIT gene expression in sporadic colorectaladenocarcinomas
    SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    
    C. Luceri et al., "Clinicopathologic features and FHIT gene expression in sporadic colorectaladenocarcinomas", SC J GASTR, 35(6), 2000, pp. 637-641
36. Sastre-Garau, X; Favre, M; Couturier, J; Orth, G
    Distinct patterns of alteration of myc genes associated with integration of human papillomavirus type 16 or type 45 DNA in two genital tumours
    JOURNAL OF GENERAL VIROLOGY
    
    X. Sastre-Garau et al., "Distinct patterns of alteration of myc genes associated with integration of human papillomavirus type 16 or type 45 DNA in two genital tumours", J GEN VIROL, 81, 2000, pp. 1983-1993
37. Helland, A; Kraggerud, SM; Kristensen, GB; Holm, R; Abeler, VM; Huebner, K; Borresen-Dale, AL; Lothe, RA
    Primary cervical carcinomas show 2 common regions of deletion at 3P, 1 within the FHIT gene: Evaluation of allelic imbalance at FHIT, RB1 and TP53 inrelation to survival
    INTERNATIONAL JOURNAL OF CANCER
    
    A. Helland et al., "Primary cervical carcinomas show 2 common regions of deletion at 3P, 1 within the FHIT gene: Evaluation of allelic imbalance at FHIT, RB1 and TP53 inrelation to survival", INT J CANC, 88(2), 2000, pp. 217-222
38. Bednarek, AK; Laflin, KJ; Daniel, RL; Liao, QY; Hawkins, KA; Aldaz, CM
    WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer
    CANCER RESEARCH
    
    A.K. Bednarek et al., "WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer", CANCER RES, 60(8), 2000, pp. 2140-2145
39. Yuan, BZ; Keck-Waggoner, C; Zimonjic, DB; Thorgeirsson, SS; Popescu, NC
    Alterations of the FHIT gene in human hepatocellular carcinoma
    CANCER RESEARCH
    
    B.Z. Yuan et al., "Alterations of the FHIT gene in human hepatocellular carcinoma", CANCER RES, 60(4), 2000, pp. 1049-1053
40. Weisberg, E; Griffin, JD
    Mechanism of resistance to the ABL tyrosine kinase inhibitor STI571 in BCR/ABL-transformed hematopoietic cell lines
    BLOOD
    
    E. Weisberg e J.D. Griffin, "Mechanism of resistance to the ABL tyrosine kinase inhibitor STI571 in BCR/ABL-transformed hematopoietic cell lines", BLOOD, 95(11), 2000, pp. 3498-3505
41. Carme, F; Rosa, M; Josep, E
    Chromosome aberrations induced by aphidicolin
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    
    F. Carme et al., "Chromosome aberrations induced by aphidicolin", MUT RES-F M, 430(1), 1999, pp. 47-53
42. Adinolfi, S; Bagni, C; Musco, G; Gibson, T; Mazzarella, L; Pastore, A
    Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains
    RNA-A PUBLICATION OF THE RNA SOCIETY
    
    S. Adinolfi et al., "Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains", RNA, 5(9), 1999, pp. 1248-1258
43. Russo, C; Rocco, L; Stingo, V; Aprea, G; Odierna, G
    A cytogenetic analysis of Gambusia holbrooki (Cyprinodontiformes, Poecilidae) from the River Sarno
    ITALIAN JOURNAL OF ZOOLOGY
    
    C. Russo et al., "A cytogenetic analysis of Gambusia holbrooki (Cyprinodontiformes, Poecilidae) from the River Sarno", ITAL J ZOOL, 66(3), 1999, pp. 291-296
44. Rithidech, KN; Cronkite, EP; Bond, VP
    Advantages of the CBA mouse in leukemogenesis research
    BLOOD CELLS MOLECULES AND DISEASES
    
    K.N. Rithidech et al., "Advantages of the CBA mouse in leukemogenesis research", BL CELL M D, 25(3), 1999, pp. 38-46
45. Hallas, C; Albitar, M; Letofsky, J; Keating, MJ; Huebner, K; Croce, CM
    Loss of FHIT expression in acute lymphoblastic leukemia
    CLINICAL CANCER RESEARCH
    
    C. Hallas et al., "Loss of FHIT expression in acute lymphoblastic leukemia", CLIN CANC R, 5(9), 1999, pp. 2409-2414
46. Schwab, M
    Oncogene amplification in solid tumors
    SEMINARS IN CANCER BIOLOGY
    
    M. Schwab, "Oncogene amplification in solid tumors", SEM CANC B, 9(4), 1999, pp. 319-325
47. Autiero, M; Culerrier, R; Bouchier, C; Basmaciogullari, S; Gaubin, M; El Marhomy, S; Blanchet, P; Paradis, V; Jardin, A; Guardiola, J; Piatier-Tonneau, D
    Abnormal restriction pattern of PIP gene associated with human primary prostate cancers
    DNA AND CELL BIOLOGY
    
    M. Autiero et al., "Abnormal restriction pattern of PIP gene associated with human primary prostate cancers", DNA CELL B, 18(6), 1999, pp. 481-487
48. Hocking, T; Feichtinger, W; Schmid, M; Haan, EA; Baker, E; Sutherland, GR
    Homozygotes for FRA16B are normal
    CHROMOSOME RESEARCH
    
    T. Hocking et al., "Homozygotes for FRA16B are normal", CHROMOS RES, 7(7), 1999, pp. 553-556
49. Ashley-Koch, A; Wolpert, CM; Menold, MM; Zaeem, L; Basu, S; Donnelly, SL; Ravan, SA; Powell, CM; Qumsiyeh, MB; Aylsworth, AS; Vance, JM; Gilbert, JR; Wright, HH; Abramson, RK; DeLong, GR; Cuccaro, ML; Pericak-Vance, MA
    Genetic studies of autistic disorder and chromosome 7
    GENOMICS
    
    A. Ashley-Koch et al., "Genetic studies of autistic disorder and chromosome 7", GENOMICS, 61(3), 1999, pp. 227-236
50. Croce, CM; Sozzi, G; Huebner, K
    Role of FHIT in human cancer
    JOURNAL OF CLINICAL ONCOLOGY
    
    C.M. Croce et al., "Role of FHIT in human cancer", J CL ONCOL, 17(5), 1999, pp. 1618-1624
51. Makinen, A; Andersson, M; Hakkinen, A; Kuosmanen, S
    A reciprocal translocation between autosomes 8 and 10 in a boar used for artificial insemination service and its effects on litter size
    ANIMAL REPRODUCTION SCIENCE
    
    A. Makinen et al., "A reciprocal translocation between autosomes 8 and 10 in a boar used for artificial insemination service and its effects on litter size", ANIM REPROD, 56(3-4), 1999, pp. 237-243
52. Hou, CD; Chiang, JT; Tai, JJ
    Testing the nonrandomness of chromosomal breakpoints using highest observed breakages
    HUMAN GENETICS
    
    C.D. Hou et al., "Testing the nonrandomness of chromosomal breakpoints using highest observed breakages", HUM GENET, 104(4), 1999, pp. 350-355
53. Melnyk, S; Pogribna, M; Miller, BJ; Basnakian, AG; Pogribny, IP; James, SJ
    Uracil misincorporation, DNA strand breaks, and gene amplification are associated with tumorigenic cell transformation in folate deficient/repleted Chinese hamster ovary cells
    CANCER LETTERS
    
    S. Melnyk et al., "Uracil misincorporation, DNA strand breaks, and gene amplification are associated with tumorigenic cell transformation in folate deficient/repleted Chinese hamster ovary cells", CANCER LETT, 146(1), 1999, pp. 35-44
54. Park, JS; Dong, SM; Kim, HS; Lee, JY; Um, SJ; Park, IS; Kim, SJ; Namkoong, SE
    Detection of p16 gene alteration in cervical cancer using tissue microdissection and LOH study
    CANCER LETTERS
    
    J.S. Park et al., "Detection of p16 gene alteration in cervical cancer using tissue microdissection and LOH study", CANCER LETT, 136(1), 1999, pp. 101-108
55. Luft, F; Gebert, J; Schneider, A; Melsheimer, P; Doeberitz, MV
    Frequent allelic imbalance of tumor suppressor gene loci in cervical dysplasia
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    
    F. Luft et al., "Frequent allelic imbalance of tumor suppressor gene loci in cervical dysplasia", INT J GYN P, 18(4), 1999, pp. 374-380
56. Peschka, B; Leygraaf, J; van der Ven, K; Montag, M; Schartmann, B; Schubert, R; van der Ven, H; Schwanitz, G
    Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection
    HUMAN REPRODUCTION
    
    B. Peschka et al., "Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection", HUM REPR, 14(9), 1999, pp. 2257-2263
57. Ilyinskikh, NN; Ilyinskikh, IN; Ilyinskikh, EN
    Chromosome breakage at sites of oncogenes in a population accidentally exposed to radioactive chemical pollution
    MUTAGENESIS
    
    N.N. Ilyinskikh et al., "Chromosome breakage at sites of oncogenes in a population accidentally exposed to radioactive chemical pollution", MUTAGENESIS, 14(1), 1999, pp. 83-86
58. Nesina, IP; Polishchuk, LZ
    Human chromosomal fragile sites and malignant tumours
    EXPERIMENTAL ONCOLOGY
    
    I.P. Nesina e L.Z. Polishchuk, "Human chromosomal fragile sites and malignant tumours", EXP ONCOL, 21(3-4), 1999, pp. 195-206
59. Schwab, M
    From fish to FISH: the comparative pathology of neuroblastomas in humans, mice and fish
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    
    M. Schwab, "From fish to FISH: the comparative pathology of neuroblastomas in humans, mice and fish", J CANC RES, 125(3-4), 1999, pp. 141-149
60. Karkera, JD; Balan, KV; Yoshikawa, T; Lipman, TO; Korman, L; Sharma, A; Patterson, RH; Sani, N; Detera-Wadleigh, SD; Wadleigh, RG
    Systematic screening of chromosome 18 for loss of heterozygosity in esophageal squamous cell carcinoma
    CANCER GENETICS AND CYTOGENETICS
    
    J.D. Karkera et al., "Systematic screening of chromosome 18 for loss of heterozygosity in esophageal squamous cell carcinoma", CANC GENET, 111(1), 1999, pp. 81-86
61. Vernole, P; Tullio, A; Caporossi, D; Didona, B; Melino, G; Tedeschi, B
    Bleomycin-induced chromosome aberrations in lymphocytes derived from patients with lamellar ichthyosis
    CANCER GENETICS AND CYTOGENETICS
    
    P. Vernole et al., "Bleomycin-induced chromosome aberrations in lymphocytes derived from patients with lamellar ichthyosis", CANC GENET, 108(2), 1999, pp. 154-157
62. Maitra, A; Wistuba, II; Gibbons, D; Gazdar, AF; Albores-Saavedra, J
    Allelic losses at chromosome 3p are seen in human papilloma virus 16 associated transitional cell carcinoma of the cervix
    GYNECOLOGIC ONCOLOGY
    
    A. Maitra et al., "Allelic losses at chromosome 3p are seen in human papilloma virus 16 associated transitional cell carcinoma of the cervix", GYNECOL ONC, 74(3), 1999, pp. 361-368
63. Balci, A; Ekmekc, A; Cetin, R
    The expression of common fragile sites in peripheral blood lymphocytes of breast and colorectal cancer patients with aphidicolin
    TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
    
    A. Balci et al., "The expression of common fragile sites in peripheral blood lymphocytes of breast and colorectal cancer patients with aphidicolin", TOH J EX ME, 189(2), 1999, pp. 107-116
64. Mitra, AB
    Genetic deletion and human papillomavirus infection in cervical cancer: Loss of heterozygosity sites at 3p and 5p are important genetic events
    INTERNATIONAL JOURNAL OF CANCER
    
    A.B. Mitra, "Genetic deletion and human papillomavirus infection in cervical cancer: Loss of heterozygosity sites at 3p and 5p are important genetic events", INT J CANC, 82(3), 1999, pp. 322-324
65. Guven, GS; Hacihanefioglu, S; Cenani, A
    Expression of aphidicolin, FUdR and caffeine-induced fragile sites in lymphocytes of healthy Turkish individuals
    GENETICA
    
    G.S. Guven et al., "Expression of aphidicolin, FUdR and caffeine-induced fragile sites in lymphocytes of healthy Turkish individuals", GENETICA, 105(1), 1999, pp. 109-116
66. Velickovic, M; Delahunt, B; Grebe, SKG
    Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus
    CANCER RESEARCH
    
    M. Velickovic et al., "Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus", CANCER RES, 59(6), 1999, pp. 1323-1326
67. Koopman, LA; Szuhai, K; van Eendenburg, JDH; Bezrookove, V; Kenter, GG; Schuuring, E; Tanke, H; Fleuren, GJ
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68. Monni, O; Zhu, Y; Franssila, K; Oinonen, R; Hoglund, P; Elonen, E; Joensuu, H; Knuutila, S
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    BRITISH JOURNAL OF HAEMATOLOGY
    
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69. BOUFFLER SD
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    Mutation research. Fundamental and molecular mechanisms of mutagenesis
    
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70. SIMI S; ATTOLINI C; GIULOTTO E
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71. SIMI S; SIMILI M; BONATTI S; CAMPAGNA M; ABBONDANDOLO A
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    Mutation research. Fundamental and molecular mechanisms of mutagenesis
    
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72. CHOW M; KOO J; NG P; RUBIN H
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73. Colls, P; Martinez-Pasarell, O; Perez, MM; Egozcue, J; Templado, C
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74. BIECHE I; LATIL A; BECETTE V; LIDEREAU R
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    Genes chromosomes & cancer (Print)
    
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75. LEBEAU MM; DRABKIN H; GLOVER TW; GEMMILL R; RASSOOL FV; MCKEITHAN TW; SMITH DI
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    Genes, chromosomes & cancer
    
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76. CASTRO PD; FAIRMAN J; NAGARAJAN L
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77. RIVADENEIRA ED; POPESCU NC; ZIMONJIC DB; CHENG GS; NELSON PJ; ROSS MD; DIPAOLO JA; KLOTMAN ME
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    International journal of oncology
    
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78. SMITH DI; HUANG HJ; WANG L
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    International journal of oncology
    
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79. Ott, G; Haaf, T; Schmid, M
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80. BERGTHORSSON JT; JOHANNSDOTTIR J; JONASDOTTIR A; EIRIKSDOTTIR G; EGILSSON V; INGVARSSON S; BARKARDOTTIR RB; ARASON A
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    European journal of cancer
    
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81. MANGANO R; PIDDINI E; CARRAMUSA L; DUHIG T; FEO S; FRIED M
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82. MATTHIAS C; BOCKMUHL U; JAHNKE V; PETERSEN I; DIETEL M; FRYER A; STRANGE RC
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83. RUFFIN MT; LANCASTER WD
    CLINICAL-MODELS OF CHEMOPREVENTION FOR CERVICAL-CANCER
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84. NICKERSON E; NELSON DL
    MOLECULAR DEFINITION OF PERICENTRIC-INVERSION BREAKPOINTS OCCURRING DURING THE EVOLUTION OF HUMANS AND CHIMPANZEES
    Genomics (San Diego, Calif.)
    
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85. SLENTZKESLER KA; HALE LP; KAUFMAN RE
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    Genomics
    
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86. Di Berardino, D; Burguete, I
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    CYTOGENETICS AND CELL GENETICS
    
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87. EGELI U
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88. Cecener, G; Egeli, U; Tasdelen, I; Tunca, B; Duman, H; Kizil, A
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    TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS
    
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89. COLLS P; MARTINEZPASARELL O; PEREZ MM; EGOZCUE J; TEMPLADO C
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90. RADHA S; NATARAJAN AT
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    Mutagenesis
    
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91. PIPIRAS E; COQUELLE A; BIETH A; DEBATISSE M
    INTERSTITIAL DELETIONS AND INTRACHROMOSOMAL AMPLIFICATION INITIATED FROM A DOUBLE-STRAND BREAK TARGETED TO A MAMMALIAN CHROMOSOME
    EMBO journal
    
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92. KOLIALEXI A; MAVROU A; TSENGHI C; TSANGARIS GT; DAFERMOU E; TZORTZATOU F; POLYCHRONOPOULOU S; HAIDAS S; METAXOTOU C
    CHROMOSOME FRAGILITY AND PREDISPOSITION TO CHILDHOOD MALIGNANCIES
    Anticancer research
    
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93. TRIVEDI AH; ROY SK; BHACHECH SH; PATEL RK; DALAL AA; BHATAVDEKAR JM; PATEL DD
    CYTOGENETIC EVALUATION OF 20 SPORADIC BREAST-CANCER PATIENTS AND THEIR FIRST-DEGREE RELATIVES
    Breast cancer research and treatment
    
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94. RAO NM; PAI SA; SHINDE SR; GHOSH SN
    REDUCED DNA-REPAIR CAPACITY IN BREAST-CANCER PATIENTS AND UNAFFECTED INDIVIDUALS FROM BREAST-CANCER FAMILIES
    Cancer genetics and cytogenetics
    
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95. SISLEY K; BRAND C; PARSONS MA; MALTBY E; REES RC; RENNIE IG
    CYTOGENETICS OF IRIS MELANOMAS - DISPARITY WITH OTHER UVEAL TRACT MELANOMAS
    Cancer genetics and cytogenetics
    
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96. MICHAELIS RC; VELAGALETI GVN; JONES C; PIVNICK EK; PHELAN MC; BOYD E; TARLETON J; WILROY RS; TUNNACLIFFE A; THARAPEL AT
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    American journal of medical genetics
    
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97. Huebner, K; Garrison, PN; Barnes, LD; Croce, CM
    The role of the FHIT/FRA3B locus in cancer
    ANNUAL REVIEW OF GENETICS
    
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98. SMITH MDA; BORSATTO B
    DOWNS-SYNDROME, AGING AND FRAGILE SITES
    Mechanism of ageing and development
    
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99. PINEAU P; MARCHIO A; MATTEI MG; KIM WH; YOUN JK; TIOLLAIS P; DEJEAN A
    EXTENSIVE ANALYSIS OF DUPLICATED-INVERTED HEPATITIS-B VIRUS INTEGRATIONS IN HUMAN HEPATOCELLULAR-CARCINOMA
    Journal of General Virology
    
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100. MANGEL L; TERNES T; SCHMITZ B; DOERFLER W
     NEW 5'-(CGG)(N)-3' REPEATS IN THE HUMAN GENOME
     The Journal of biological chemistry
     
     L. Mangel et al., "NEW 5'-(CGG)(N)-3' REPEATS IN THE HUMAN GENOME", The Journal of biological chemistry, 273(46), 1998, pp. 30466-30471