메뉴 건너뛰기




Volumn 38, Issue 4, 1996, Pages 291-296

Clonal chromosome abnormalities in Fanconi anemia

Author keywords

chromosomal abnormalities; clonal abnormalities; Fanconi anemia; leukemias; myelodysplastic syndrome

Indexed keywords

CELL CLONE; CHROMOSOME ABERRATION; FANCONI ANEMIA; HUMAN; LEUKEMIA; MYELODYSPLASTIC SYNDROME; REVIEW;

EID: 0029786036     PISSN: 14302772     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00282-996-0291-6     Document Type: Review
Times cited : (10)

References (69)
  • 1
    • 0026607986 scopus 로고
    • Fanconi,s anemia. Current concepts
    • Alter BP (1992) Fanconi,s anemia. Current concepts. Am J Pediatr Hematol Oncol 14 : 170-176
    • (1992) Am J Pediatr Hematol Oncol , vol.14 , pp. 170-176
    • Alter, B.P.1
  • 2
    • 0026571927 scopus 로고
    • Leukemia and preleukemia in Fanconi's anemia
    • Alter BP (1992) Leukemia and preleukemia in Fanconi's anemia. Cancer Genet Cytogenet 58 : 206-208
    • (1992) Cancer Genet Cytogenet , vol.58 , pp. 206-208
    • Alter, B.P.1
  • 3
    • 0027445492 scopus 로고
    • Fanconi's anaemia and its variability
    • Alter BP (1993) Fanconi's anaemia and its variability. Br J Haematol 85 : 1-9
    • (1993) Br J Haematol , vol.85 , pp. 1-9
    • Alter, B.P.1
  • 4
    • 0027507581 scopus 로고
    • Clonal chromosomal abnormalities in Fanconi's anaemia: What do they really mean?
    • Alter BP, Scalise A, McCombs J, et al (1993) Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean? Br J Haematol 85 : 627-630
    • (1993) Br J Haematol , vol.85 , pp. 627-630
    • Alter, B.P.1    Scalise, A.2    McCombs, J.3
  • 5
    • 0026604026 scopus 로고
    • Fanconi anemia and leukemia: Tracking the genes
    • Auerbach AD (1992) Fanconi anemia and leukemia: Tracking the genes (abstract). Leukemia 6 [Suppl 2] : 1-4
    • (1992) Leukemia , vol.6 , Issue.2 SUPPL. , pp. 1-4
    • Auerbach, A.D.1
  • 6
    • 0025959243 scopus 로고
    • Leukemia and preleukemia in Fanconi anemia patients
    • Auerbach AD, Allen RG (1991): Leukemia and preleukemia in Fanconi anemia patients. Cancer Genet Cytogenet 51 : 1-12
    • (1991) Cancer Genet Cytogenet , vol.51 , pp. 1-12
    • Auerbach, A.D.1    Allen, R.G.2
  • 7
    • 0024543636 scopus 로고
    • International Fanconi anemia registry: Relation of clinical symptoms to diepoxybutane sensitivity
    • Auerbach AD, Rogatko A, Schroeder-Kurth TM (1989) International Fanconi anemia registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood 73 : 391-396
    • (1989) Blood , vol.73 , pp. 391-396
    • Auerbach, A.D.1    Rogatko, A.2    Schroeder-Kurth, T.M.3
  • 8
    • 0018608391 scopus 로고
    • Carcinogen-induced chromosome breakage in chromosome instability syndromes
    • Auerbach AD, Wolman SR (1979) Carcinogen-induced chromosome breakage in chromosome instability syndromes. Cancer Genet Cytogenet 1 : 21-28
    • (1979) Cancer Genet Cytogenet , vol.1 , pp. 21-28
    • Auerbach, A.D.1    Wolman, S.R.2
  • 9
    • 0019365249 scopus 로고
    • Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method
    • Auerbach AD, Adler B, Chaganti RSK (1981) Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method. Pediatrics 67 : 128-135
    • (1981) Pediatrics , vol.67 , pp. 128-135
    • Auerbach, A.D.1    Adler, B.2    Chaganti, R.S.K.3
  • 10
    • 0020083491 scopus 로고
    • Acute myeloid leukemia as the first hematologic manifestation of Fanconi anemia
    • Auerbach AD, Weiner MA, Warbuton D, et al (1982) Acute myeloid leukemia as the first hematologic manifestation of Fanconi anemia. Am J Hematol 12 : 289-300
    • (1982) Am J Hematol , vol.12 , pp. 289-300
    • Auerbach, A.D.1    Weiner, M.A.2    Warbuton, D.3
  • 11
    • 0024467996 scopus 로고
    • Cutaneous and extracutaneous neutrophilic infiltrates (Sweet syndrome) in three patients with Fanconi anemia
    • Baron F, Sybert VP, Andrews RG (1989) Cutaneous and extracutaneous neutrophilic infiltrates (Sweet syndrome) in three patients with Fanconi anemia. J Pediatr 115 : 726-729
    • (1989) J Pediatr , vol.115 , pp. 726-729
    • Baron, F.1    Sybert, V.P.2    Andrews, R.G.3
  • 12
    • 0023184631 scopus 로고
    • Preleukemia in Fanconi's anemia: Hematopoietic cell multinuclearity, membrane duplication, and dysgranulogenesis
    • Barton IC, Parmley RT, Carroll AJ, et al (1987) Preleukemia in Fanconi's anemia: Hematopoietic cell multinuclearity, membrane duplication, and dysgranulogenesis. J Submicrosc Cytol 19 : 355-364
    • (1987) J Submicrosc Cytol , vol.19 , pp. 355-364
    • Barton, I.C.1    Parmley, R.T.2    Carroll, A.J.3
  • 13
    • 0018973190 scopus 로고
    • Chromosomal studies of leukemic and preleukemic Fanconi's anemia patients
    • Berger R, Bernheim A, Le Coniat M, et al (1980) Chromosomal studies of leukemic and preleukemic Fanconi's anemia patients. Hum Genet 56 : 59-62
    • (1980) Hum Genet , vol.56 , pp. 59-62
    • Berger, R.1    Bernheim, A.2    Le Coniat, M.3
  • 14
    • 0019258970 scopus 로고
    • Nitrogen mustard-induced chromosome breakage: A tool for Fanconi's anemia diagnosis
    • Berger R, Bernheim A, Le Coniat M, et al (1980) Nitrogen mustard-induced chromosome breakage: a tool for Fanconi's anemia diagnosis. Cancer Genet Cytogenet 2 : 269-274
    • (1980) Cancer Genet Cytogenet , vol.2 , pp. 269-274
    • Berger, R.1    Bernheim, A.2    Le Coniat, M.3
  • 15
    • 0016677602 scopus 로고
    • Anomalies chromosomiques et anémie de Fanconi. Etude de 4 cas
    • Berger R, Bussel A, Schenmetzler C (1975) Anomalies chromosomiques et anémie de Fanconi. Etude de 4 cas. Nouv Rev Fr Hematol 15 : 539-550
    • (1975) Nouv Rev Fr Hematol , vol.15 , pp. 539-550
    • Berger, R.1    Bussel, A.2    Schenmetzler, C.3
  • 16
    • 0017736598 scopus 로고
    • Somatic segregation and Fanconi anemia
    • Berger R, Bussel A, Schenmetzler C (1977) Somatic segregation and Fanconi anemia. Clin Genet 11 : 409-415
    • (1977) Clin Genet , vol.11 , pp. 409-415
    • Berger, R.1    Bussel, A.2    Schenmetzler, C.3
  • 17
    • 0012782302 scopus 로고
    • Cytogenetic studies in Fanconi anemia: Induced chromosomal breakage and cytogenetics of leukemia
    • TM Schroeder-Kurth, AD Auerbach, G Obe (eds) Springer, Berlin Heidelberg New York
    • Berger R, Le Coniat M (1989) Cytogenetic studies in Fanconi anemia: induced chromosomal breakage and cytogenetics of leukemia. In : TM Schroeder-Kurth, AD Auerbach, G Obe (eds) Fanconi Anemia. Clinical, Cytogenetic and Experimental aspects. Springer, Berlin Heidelberg New York, pp 93-99
    • (1989) Fanconi Anemia. Clinical, Cytogenetic and Experimental Aspects , pp. 93-99
    • Berger, R.1    Le Coniat, M.2
  • 19
    • 0027468707 scopus 로고
    • Chromosome abnormalities in bone marrow of Fanconi anemia patients
    • Berger R, Le Coniat M, Schaison G (1993) Chromosome abnormalities in bone marrow of Fanconi anemia patients. Cancer Genet Cytogenet 65 : 47-50
    • (1993) Cancer Genet Cytogenet , vol.65 , pp. 47-50
    • Berger, R.1    Le Coniat, M.2    Schaison, G.3
  • 20
    • 0024390669 scopus 로고
    • Chronic myelomonocytic leukemia with chromosomal changes involving 1p36 and hepatocellular carcinoma in a case of Fanconi's anemia
    • Bessho F, Mizutani S, Hayashi Y, et al (1989) Chronic myelomonocytic leukemia with chromosomal changes involving 1p36 and hepatocellular carcinoma in a case of Fanconi's anemia. Eur J Haematol 42: 492-495
    • (1989) Eur J Haematol , vol.42 , pp. 492-495
    • Bessho, F.1    Mizutani, S.2    Hayashi, Y.3
  • 21
    • 0017349665 scopus 로고
    • Fanconi anemia leading to acute myelomonocytic leukemia
    • Bourgeois CA, Hill FGH (1977) Fanconi anemia leading to acute myelomonocytic leukemia. Cancer 39 : 1163-1167
    • (1977) Cancer , vol.39 , pp. 1163-1167
    • Bourgeois, C.A.1    Hill, F.G.H.2
  • 22
    • 0029410634 scopus 로고
    • Complementation groups: One or more per gene?
    • Buchwald M (1995) Complementation groups: one or more per gene? Nat Genet 11 : 228-230
    • (1995) Nat Genet , vol.11 , pp. 228-230
    • Buchwald, M.1
  • 23
    • 0028068579 scopus 로고
    • Hematologic abnormalities in Fanconi anemia: An international Fanconi anemia registry study
    • Butturini A, Gale RP, Verlander PC, et al (1994) Hematologic abnormalities in Fanconi anemia: An international Fanconi anemia registry study. Blood 84 : 1650-1655
    • (1994) Blood , vol.84 , pp. 1650-1655
    • Butturini, A.1    Gale, R.P.2    Verlander, P.C.3
  • 24
    • 0019378276 scopus 로고
    • Mitomycin C test for disgnostic differentiation of idiopathic aplastic anemia and Fanconi anemia
    • Cervenka J, Arthur D, Yasis C (1981) Mitomycin C test for disgnostic differentiation of idiopathic aplastic anemia and Fanconi anemia. Pediatrics 67 : 119-127
    • (1981) Pediatrics , vol.67 , pp. 119-127
    • Cervenka, J.1    Arthur, D.2    Yasis, C.3
  • 25
    • 13344278020 scopus 로고    scopus 로고
    • Inactivation of Fac in mice produces chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
    • Chen M, Tomkins DJ, Auerbach W, et al (1996) Inactivation of Fac in mice produces chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. Nat Genet 12 : 448-451
    • (1996) Nat Genet , vol.12 , pp. 448-451
    • Chen, M.1    Tomkins, D.J.2    Auerbach, W.3
  • 26
    • 0020974131 scopus 로고
    • Investigation of the cell cycle response of normal and Fanconi's anaemia fibroblasts to nitrogen mustard using flow cytometry
    • Dean SW, Fox M (1983) Investigation of the cell cycle response of normal and Fanconi's anaemia fibroblasts to nitrogen mustard using flow cytometry J Cell Sci 64 : 265-279
    • (1983) J Cell Sci , vol.64 , pp. 265-279
    • Dean, S.W.1    Fox, M.2
  • 27
    • 0021925626 scopus 로고
    • Identification of two complementation groups in Fanconi anemia
    • Duckworth-Rysiecki G, Cornish K, et al (1985) Identification of two complementation groups in Fanconi anemia. Somat Cell Mol Genet 11 : 35-41
    • (1985) Somat Cell Mol Genet , vol.11 , pp. 35-41
    • Duckworth-Rysiecki, G.1    Cornish, K.2
  • 28
    • 0020307710 scopus 로고
    • The cell cycle of lymphocytes in Fanconi's anemia
    • Dutrillaux B, Aurias A, Fosse A-M, et al (1982) The cell cycle of lymphocytes in Fanconi's anemia. Hum Genet 62 : 327-332
    • (1982) Hum Genet , vol.62 , pp. 327-332
    • Dutrillaux, B.1    Aurias, A.2    Fosse, A.-M.3
  • 29
    • 0027339986 scopus 로고
    • 554-to-pro substitution completely abolishes activity of the Fanconi anemia (FCC) protein
    • 554-to-pro substitution completely abolishes activity of the Fanconi anemia (FCC) protein. Hum Mol Genet 2 : 123-126
    • (1993) Hum Mol Genet , vol.2 , pp. 123-126
    • Gavish, H.1    Dos Santoss, C.C.2    Buchwald, M.3
  • 30
    • 0027299882 scopus 로고
    • A nonsense mutation and exon skipping in the Fanconi anaemia group C gene
    • Gibson RA, Hajianpour A, Murer-Orlando M, et al (1993) A nonsense mutation and exon skipping in the Fanconi anaemia group C gene. Hum Mol Genet 2 : 797-799
    • (1993) Hum Mol Genet , vol.2 , pp. 797-799
    • Gibson, R.A.1    Hajianpour, A.2    Murer-Orlando, M.3
  • 31
    • 0027165838 scopus 로고
    • A damage-recogniion protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation goup A, cells
    • Hang B, Yeung AT, Lambert MW (1993) A damage-recogniion protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation goup A, cells. Nucleic Acids Res 21 : 418-4192
    • (1993) Nucleic Acids Res , vol.21 , pp. 418-4192
    • Hang, B.1    Yeung, A.T.2    Lambert, M.W.3
  • 32
    • 0022545156 scopus 로고
    • Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia
    • Huret J-L, Benz E, Guilhot F, Brizard A, Tanzer J (1986) Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia. Hum Genet 74 : 98-100
    • (1986) Hum Genet , vol.74 , pp. 98-100
    • Huret, J.-L.1    Benz, E.2    Guilhot, F.3    Brizard, A.4    Tanzer, J.5
  • 33
    • 0024274295 scopus 로고
    • Karyotype evolution of a patient with Fanconi anemia: Breakpoints in clonal anomalies of this disease
    • Huret J-L, Tanzer J, Guilhot F, et al (1988) Karyotype evolution of a patient with Fanconi anemia: breakpoints in clonal anomalies of this disease. Cytogenet Cell Genet 48 : 224-227
    • (1988) Cytogenet Cell Genet , vol.48 , pp. 224-227
    • Huret, J.-L.1    Tanzer, J.2    Guilhot, F.3
  • 34
    • 0029163523 scopus 로고
    • Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype
    • Joenje H, Lo Ten Foe JR, Oostra AB, et al (1995) Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype. Blood 86 : 2156-2160
    • (1995) Blood , vol.86 , pp. 2156-2160
    • Joenje, H.1    Lo Ten Foe, J.R.2    Oostra, A.B.3
  • 35
    • 0030047192 scopus 로고    scopus 로고
    • Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients
    • Krasnoshtein F, Buchwald M (1996) Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients. Hum Mol Genet 5 : 5-93
    • (1996) Hum Mol Genet , vol.5 , pp. 5-93
    • Krasnoshtein, F.1    Buchwald, M.2
  • 36
    • 0019986506 scopus 로고
    • Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia
    • Latt SA, Kaiser SA, Lojewski A, et al (1982) Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia. Cytogenet Cell Genet 33 : 133-138
    • (1982) Cytogenet Cell Genet , vol.33 , pp. 133-138
    • Latt, S.A.1    Kaiser, S.A.2    Lojewski, A.3
  • 37
    • 0016264916 scopus 로고
    • Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution
    • Lisker R, Cobo de Gutiérrez A (1974) Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution. Clin Genet 5 : 72-76
    • (1974) Clin Genet , vol.5 , pp. 72-76
    • Lisker, R.1    Cobo De Gutiérrez, A.2
  • 38
    • 0028109326 scopus 로고
    • Fanconi anemia and novel strategies for therapy
    • Liu JM, Buchwald M, Walsh CE, et al (1994) Fanconi anemia and novel strategies for therapy. Blood 84 : 3995-4007
    • (1994) Blood , vol.84 , pp. 3995-4007
    • Liu, J.M.1    Buchwald, M.2    Walsh, C.E.3
  • 39
    • 0029002645 scopus 로고
    • Retroviral-mediated transduction of the Fanconi anemia C complementing (FACC) gene in two murine transplantation models
    • Liu JM, Kim S, Walsch CE (1995) Retroviral-mediated transduction of the Fanconi anemia C complementing (FACC) gene in two murine transplantation models. Blood Cells Mol Dis 21 : 56-63
    • (1995) Blood Cells Mol Dis , vol.21 , pp. 56-63
    • Liu, J.M.1    Kim, S.2    Walsch, C.E.3
  • 41
    • 0026100399 scopus 로고
    • Fanconi anemia: Evidence for linkage heterogeneity on chromosome 20q
    • Mann WR, Venkatraj VS, Allen RG, et al (1991) Fanconi anemia: evidence for linkage heterogeneity on chromosome 20q. Genomics 9 : 329-337
    • (1991) Genomics , vol.9 , pp. 329-337
    • Mann, W.R.1    Venkatraj, V.S.2    Allen, R.G.3
  • 42
    • 0026026127 scopus 로고
    • A simple diagnostic test for Fanconi anemia by flow cytometry
    • Miglierina R, Le Coniat M, Berger R (1991) A simple diagnostic test for Fanconi anemia by flow cytometry. Anal Cell Pathol 3 : 111-118
    • (1991) Anal Cell Pathol , vol.3 , pp. 111-118
    • Miglierina, R.1    Le Coniat, M.2    Berger, R.3
  • 44
    • 0012770816 scopus 로고
    • Anomalies cytogénétiques clonales dans l'anémie de Fanconi
    • Mozziconacci MJ, Arnoulet C, Stoppa AM, et al (1995) Anomalies cytogénétiques clonales dans l'anémie de Fanconi. Nouv Rev Fr Hematol 37 : 52-53
    • (1995) Nouv Rev Fr Hematol , vol.37 , pp. 52-53
    • Mozziconacci, M.J.1    Arnoulet, C.2    Stoppa, A.M.3
  • 45
    • 0021688628 scopus 로고
    • Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia
    • Nowell P, Bergman G, Besa E, et al (1984) Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia. Blood 64 : 1135-1138
    • (1984) Blood , vol.64 , pp. 1135-1138
    • Nowell, P.1    Bergman, G.2    Besa, E.3
  • 46
    • 0019221372 scopus 로고
    • Fanconi anemia. Oxymetholone hepatic tumors, and chromosome aberrations associated with leukemic transition
    • Obeid DA, Hill FGH, Harnden D, et al (1980) Fanconi anemia. Oxymetholone hepatic tumors, and chromosome aberrations associated with leukemic transition. Cancer 46 : 1401-1404
    • (1980) Cancer , vol.46 , pp. 1401-1404
    • Obeid, D.A.1    Hill, F.G.H.2    Harnden, D.3
  • 47
    • 0028840709 scopus 로고
    • Localisation of the Fanconi anaemia complementation group A gene to 16q24.3
    • Pronk JC, Gibson RA, Savoia A, et al (1995) Localisation of the Fanconi anaemia complementation group A gene to 16q24.3 Nat Genet 11 : 338-340
    • (1995) Nat Genet , vol.11 , pp. 338-340
    • Pronk, J.C.1    Gibson, R.A.2    Savoia, A.3
  • 48
    • 0020043728 scopus 로고
    • Giant marker chromosome in Fanconi's anemia transforming into erythroleukemia in an adult
    • Rotzak R, Kaplinsky N, Chaki R, et al (1982) Giant marker chromosome in Fanconi's anemia transforming into erythroleukemia in an adult. Acta Haematol 67 : 214-216
    • (1982) Acta Haematol , vol.67 , pp. 214-216
    • Rotzak, R.1    Kaplinsky, N.2    Chaki, R.3
  • 49
    • 0015891353 scopus 로고
    • A high susceptibility of Fanconi's anemia to chromosome breakage by cross-linking agents
    • Sasaki MS, Tonomura A (1973) A high susceptibility of Fanconi's anemia to chromosome breakage by cross-linking agents. Cancer Res 33 : 1824-1836
    • (1973) Cancer Res , vol.33 , pp. 1824-1836
    • Sasaki, M.S.1    Tonomura, A.2
  • 50
    • 0029057336 scopus 로고
    • A single ataxia telangiectasia gene with a product similar to PI-3 kinase
    • Savitsky K, Bar-Shira A, Gilad S, et al (1995) A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 268 : 1749-1753
    • (1995) Science , vol.268 , pp. 1749-1753
    • Savitsky, K.1    Bar-Shira, A.2    Gilad, S.3
  • 51
    • 0020579712 scopus 로고
    • L'anémie de Fanconi. Fréquence de l'évolution vers la leucémie
    • Schaison G, Leverger G, Yildiz C, et al (1983) L'anémie de Fanconi. Fréquence de l'évolution vers la leucémie. Nouv Presse Med 12 : 1269-1274
    • (1983) Nouv Presse Med , vol.12 , pp. 1269-1274
    • Schaison, G.1    Leverger, G.2    Yildiz, C.3
  • 52
    • 0023204590 scopus 로고
    • Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1q12-32 triplication) via BRDU/Hoechst flow cytometry
    • Schindler D, Kubbies M, Hoehn H, et al (1987) Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1q12-32 triplication) via BRDU/Hoechst flow cytometry. Am J Pediat Hematol Oncol 9 : 172-177
    • (1987) Am J Pediat Hematol Oncol , vol.9 , pp. 172-177
    • Schindler, D.1    Kubbies, M.2    Hoehn, H.3
  • 53
    • 0013772684 scopus 로고
    • Spontane Chromosmosomenaberrationen bei familiärer Panmyelopathie
    • Schroeder TM, Anschütz F, Knopp A (1964) Spontane Chromosmosomenaberrationen bei familiärer Panmyelopathie. Humangenetik 1 : 194-196
    • (1964) Humangenetik , vol.1 , pp. 194-196
    • Schroeder, T.M.1    Anschütz, F.2    Knopp, A.3
  • 54
    • 0028950319 scopus 로고
    • Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia
    • Seyeschab H, Friedl R, Sun Y, et al (1995) Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia. Blood 85 : 2233-2237
    • (1995) Blood , vol.85 , pp. 2233-2237
    • Seyeschab, H.1    Friedl, R.2    Sun, Y.3
  • 55
    • 0024338711 scopus 로고
    • Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anemia and selective IgA deficiency
    • Standen GR, Hughes IA, Geddes AD, et al (1989) Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anemia and selective IgA deficiency. Am J Hematol 31 : 280-283
    • (1989) Am J Hematol , vol.31 , pp. 280-283
    • Standen, G.R.1    Hughes, I.A.2    Geddes, A.D.3
  • 56
    • 0021241723 scopus 로고
    • Transformation of Fanconi's anemia to acute nonlymphocytic leukemia associated with emergence of monosomy 7
    • Stivrins TJ, Davis RB, Sanger W, et al (1984) Transformation of Fanconi's anemia to acute nonlymphocytic leukemia associated with emergence of monosomy 7. Blood 64 : 173-176
    • (1984) Blood , vol.64 , pp. 173-176
    • Stivrins, T.J.1    Davis, R.B.2    Sanger, W.3
  • 57
    • 0026878842 scopus 로고
    • Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
    • Strathdee CA, Duncan AMV, Buchwald M (1992) Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nat Genet 1 : 196-198
    • (1992) Nat Genet , vol.1 , pp. 196-198
    • Strathdee, C.A.1    Duncan, A.M.V.2    Buchwald, M.3
  • 58
    • 0026521238 scopus 로고
    • Cloning of cDNAs for Fanconi's anaemia by functional complementation
    • Strathdee CA, Gavish H, Shannon WR, et al (1992) Cloning of cDNAs for Fanconi's anaemia by functional complementation. Nature 356 : 763-767
    • (1992) Nature , vol.356 , pp. 763-767
    • Strathdee, C.A.1    Gavish, H.2    Shannon, W.R.3
  • 59
    • 0012841242 scopus 로고
    • Anomalies du chromosome 1 dans 3 cas de leucémie compliquant une aplasie de Fanconi (FA)
    • Tanzer J, Frocrain C, Desmarest MC (1980) Anomalies du chromosome 1 dans 3 cas de leucémie compliquant une aplasie de Fanconi (FA). Nouv Rev Fr Hematol 22 [Suppl XCIII]
    • (1980) Nouv Rev Fr Hematol , vol.22 , Issue.93 SUPPL.
    • Tanzer, J.1    Frocrain, C.2    Desmarest, M.C.3
  • 60
    • 0025860414 scopus 로고
    • Transient t(Y;1)(q12;q21) in a patient with Fanconi anemia and myelodysplastic syndrome
    • Thompson PW, Standen GR, Geddes AD (1991) Transient t(Y;1)(q12;q21) in a patient with Fanconi anemia and myelodysplastic syndrome. Cancer Genet Cytogenet 52 : 201-202
    • (1991) Cancer Genet Cytogenet , vol.52 , pp. 201-202
    • Thompson, P.W.1    Standen, G.R.2    Geddes, A.D.3
  • 61
    • 0028141695 scopus 로고
    • Clonality studies and N-ras and P53 mutation analysis of hematopoietic cells in Fanconi anemia
    • Venkatraj VS, Gaidaao G, Auerbach AD (1994) Clonality studies and N-ras and P53 mutation analysis of hematopoietic cells in Fanconi anemia. Leukemia 8 : 1354-1358
    • (1994) Leukemia , vol.8 , pp. 1354-1358
    • Venkatraj, V.S.1    Gaidaao, G.2    Auerbach, A.D.3
  • 62
    • 0028231738 scopus 로고
    • Mutation analysis of the Fanconi anemia gene FACC
    • Verlander PC, Lin JD, Udono MU, et al (1994) Mutation analysis of the Fanconi anemia gene FACC. Am J Hum Genet 54 : 595-601
    • (1994) Am J Hum Genet , vol.54 , pp. 595-601
    • Verlander, P.C.1    Lin, J.D.2    Udono, M.U.3
  • 63
    • 0028131245 scopus 로고
    • Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector
    • Walsh CE, Nienhuis AW, Samulski RJ, et al (1994) Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector. J Clin Invest 94 : 1440-1448
    • (1994) J Clin Invest , vol.94 , pp. 1440-1448
    • Walsh, C.E.1    Nienhuis, A.W.2    Samulski, R.J.3
  • 64
    • 0027215175 scopus 로고
    • Cloning and analysis of the murine Fanconi anemia group C cDNA
    • Wevrick R, Clarke CA, Buchwald M (1993) Cloning and analysis of the murine Fanconi anemia group C cDNA. Hum Mol Genet 2 : 655-662
    • (1993) Hum Mol Genet , vol.2 , pp. 655-662
    • Wevrick, R.1    Clarke, C.A.2    Buchwald, M.3
  • 65
    • 0028857959 scopus 로고
    • Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p
    • Whitney M, Thayer M, Reifsteck C, et al (1995) Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p. Nat Genet 11 : 341-343
    • (1995) Nat Genet , vol.11 , pp. 341-343
    • Whitney, M.1    Thayer, M.2    Reifsteck, C.3
  • 66
    • 0021967211 scopus 로고
    • Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with nonlymphocytic acute leukemia
    • Woods WC, Nesbit ME, Buckley J, et al for the Children's Cancer Study Group (1985) Correlation of chromosome abnormalities with patient characteristics, histologic subtype, and induction success in children with nonlymphocytic acute leukemia. J Clin Oncol 3 : 3-11
    • (1985) J Clin Oncol , vol.3 , pp. 3-11
    • Woods, W.C.1    Nesbit, M.E.2    Buckley, J.3
  • 67
    • 0028275031 scopus 로고
    • The Fanconi anemia polypeptide FACC is localized to the cytoplams
    • Yamashita T, Barber DL, Zhu Y, et al (1994) The Fanconi anemia polypeptide FACC is localized to the cytoplams. Proc Natl Acad Sci USA 91 : 6712-6716
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 6712-6716
    • Yamashita, T.1    Barber, D.L.2    Zhu, Y.3
  • 68
    • 0028366291 scopus 로고
    • Acute lymphoblastic leukemia in Fanconi's anemia
    • Yetgin S, Tuncer M, Güler E, et al (1994) Acute lymphoblastic leukemia in Fanconi's anemia. Am J Hematol 45 : 94
    • (1994) Am J Hematol , vol.45 , pp. 94
    • Yetgin, S.1    Tuncer, M.2    Güler, E.3
  • 69
    • 0027999023 scopus 로고
    • Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells
    • Youssoufian H (1994) Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells. Proc Natl Acad Sci USA 91 : 7975-7979
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 7975-7979
    • Youssoufian, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.