-
1
-
-
0024543159
-
Fanconi anaemia-constitutional, familial aplastic anaemia
-
Gordon EC, Rutherford TR. Fanconi anaemia-constitutional, familial aplastic anaemia. Bailleres Clin Haematol 1989; 2: 139-51.
-
(1989)
Bailleres Clin Haematol
, vol.2
, pp. 139-151
-
-
Gordon, E.C.1
Rutherford, T.R.2
-
2
-
-
0027445492
-
Fanconi's anaemia and its variability
-
Alter BP. Fanconi's anaemia and its variability. BJ Haematol 1993; 85: 9-14.
-
(1993)
BJ Haematol
, vol.85
, pp. 9-14
-
-
Alter, B.P.1
-
3
-
-
0028944751
-
Fanconi anaemia research: Current status and prospects
-
Joenje H, Mathew C, Gluckman E. Fanconi anaemia research: Current status and prospects. Eur J Cancer 1995; 31: 268-72.
-
(1995)
Eur J Cancer
, vol.31
, pp. 268-272
-
-
Joenje, H.1
Mathew, C.2
Gluckman, E.3
-
4
-
-
0030453695
-
Fanconi anemia complementation group E: Clinical and cytogenetic data of the first patient
-
Wegner RD, Henrichs Y, Joenje H, Schroeder-Kurth T. Fanconi anemia complementation group E: Clinical and cytogenetic data of the first patient. Clin Genet 1996; 50: 479-82.
-
(1996)
Clin Genet
, vol.50
, pp. 479-482
-
-
Wegner, R.D.1
Henrichs, Y.2
Joenje, H.3
Schroeder-Kurth, T.4
-
5
-
-
0026457889
-
Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: Ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome
-
Heim R, Lench N, Swiff M. Heterozygous manifestations in four autosomal recessive human cancer-prone syndromes: Ataxia telangiectasia, xeroderma pigmentosum, Fanconi anemia, and Bloom syndrome. Mutat Res 1992; 284: 25-36.
-
(1992)
Mutat Res
, vol.284
, pp. 25-36
-
-
Heim, R.1
Lench, N.2
Swiff, M.3
-
6
-
-
0347412094
-
Utilidad de la prueba de exposición de linfocitos a mitomicina C en el diagnóstico de anemia de Fanconi
-
Frías S, Carnevale A, Del Castillo V. Utilidad de la prueba de exposición de linfocitos a mitomicina C en el diagnóstico de anemia de Fanconi. Rev Invest Clin 1984; 36: 219-21.
-
(1984)
Rev Invest Clin
, vol.36
, pp. 219-221
-
-
Frías, S.1
Carnevale, A.2
Del Castillo, V.3
-
7
-
-
0011875820
-
Efecto de la cocultivación y la adición de plasma normal sobre la respuesta a la mitomicina C de los linfocitos de anemia de Fanconi
-
Carnevale A, Frias S. Efecto de la cocultivación y la adición de plasma normal sobre la respuesta a la mitomicina C de los linfocitos de anemia de Fanconi. Rev Invest Clin 1985; 37: 31-4.
-
(1985)
Rev Invest Clin
, vol.37
, pp. 31-34
-
-
Carnevale, A.1
Frias, S.2
-
8
-
-
0013772684
-
Spontaneous chromosome aberrations in familial panmyelopathy
-
Schroeder TM, Anschutz F, Knopp A. Spontaneous chromosome aberrations in familial panmyelopathy. Hum Genet 1964; 1: 194-9.
-
(1964)
Hum Genet
, vol.1
, pp. 194-199
-
-
Schroeder, T.M.1
Anschutz, F.2
Knopp, A.3
-
9
-
-
0015891353
-
A high susceptibility of Fanconi's anemia to chromosome breakage by DNA crosslinking agents
-
Sasaki MS, Tonomura A. A high susceptibility of Fanconi's anemia to chromosome breakage by DNA crosslinking agents. Cancer 1973; 33: 1829-36.
-
(1973)
Cancer
, vol.33
, pp. 1829-1836
-
-
Sasaki, M.S.1
Tonomura, A.2
-
10
-
-
0017118656
-
Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens
-
Auerbach AD, Wolman SR. Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens. Nature 1976; 261: 494-6.
-
(1976)
Nature
, vol.261
, pp. 494-496
-
-
Auerbach, A.D.1
Wolman, S.R.2
-
11
-
-
0024400730
-
Sinergismo bromodesoxiuridina-mitomicina C en la producción de aberraciones cromosómicas en anemia de Fanconi
-
Frias S, Molina B, Carnevale A. Sinergismo bromodesoxiuridina-mitomicina C en la producción de aberraciones cromosómicas en anemia de Fanconi. Rev Invest Clin 1989; 41: 31-5.
-
(1989)
Rev Invest Clin
, vol.41
, pp. 31-35
-
-
Frias, S.1
Molina, B.2
Carnevale, A.3
-
12
-
-
0026001403
-
Effect of mitomycin C and bromodeoxyuridine on Fanconi anemia lymphocytes
-
Frias S, Mendoza S, Molina B, Carnevale A. Effect of mitomycin C and bromodeoxyuridine on Fanconi anemia lymphocytes. Ann Genet 1991; 34(2): 104-7.
-
(1991)
Ann Genet
, vol.34
, Issue.2
, pp. 104-107
-
-
Frias, S.1
Mendoza, S.2
Molina, B.3
Carnevale, A.4
-
13
-
-
0027008384
-
Efecto de la adición de medios condicionados sobre la respuesta de los linfocitos de anemia de Fanconi a la mitomicina C
-
Frias S, Molina B, Gómez L, Carnevale A. Efecto de la adición de medios condicionados sobre la respuesta de los linfocitos de anemia de Fanconi a la mitomicina C. Rev Invest Clin 1992; 44: 519-24.
-
(1992)
Rev Invest Clin
, vol.44
, pp. 519-524
-
-
Frias, S.1
Molina, B.2
Gómez, L.3
Carnevale, A.4
-
14
-
-
0027861014
-
Fanconi anemia diagnosis and the diepoxibutane (DEB) test
-
Auerbach AD. Fanconi anemia diagnosis and the diepoxibutane (DEB) test. Exp Hematol 1993; 21: 731-6.
-
(1993)
Exp Hematol
, vol.21
, pp. 731-736
-
-
Auerbach, A.D.1
-
15
-
-
0023632030
-
The fate of 8-methoxy-psoralen-photoinduced DNA interstrand cross-links in Fanconi's anemia cells of defined complementation groups
-
Papadopoulo D, Averbeck D, Moustacchi E. The fate of 8-methoxy-psoralen-photoinduced DNA interstrand cross-links in Fanconi's anemia cells of defined complementation groups. Mutat Res 1987; 184: 271-7.
-
(1987)
Mutat Res
, vol.184
, pp. 271-277
-
-
Papadopoulo, D.1
Averbeck, D.2
Moustacchi, E.3
-
16
-
-
0038567069
-
Chromosomal breakage in response to cross-linking agents in the diagnosis of Fanconi anemia
-
Schroeder TM, Auerbach A and Obe G (eds). Berlin, Heidelberg: Springer-Verlag
-
Arwert F, Kwee L. Chromosomal breakage in response to cross-linking agents in the diagnosis of Fanconi anemia. In: Schroeder TM, Auerbach A and Obe G (eds). Fanconi anemia, clinical cytogenetic and experimental aspects. Berlin, Heidelberg: Springer-Verlag, 1989: 83-92.
-
(1989)
Fanconi Anemia, Clinical Cytogenetic and Experimental Aspects
, pp. 83-92
-
-
Arwert, F.1
Kwee, L.2
-
17
-
-
0020608715
-
Unusual response to bifunctional alkylating agents in a case of Fanconi anaemia
-
Kwee ML, Poll EHA, van de Kamp JJP, Koning H, Eriksson AW, Joenje H. Unusual response to bifunctional alkylating agents in a case of Fanconi anaemia. Hum Genet 1983; 64: 384-7.
-
(1983)
Hum Genet
, vol.64
, pp. 384-387
-
-
Kwee, M.L.1
Poll, E.H.A.2
Van De Kamp, J.J.P.3
Koning, H.4
Eriksson, A.W.5
Joenje, H.6
-
18
-
-
0030292447
-
Fanconi anaemia forges a novel pathway
-
D'Andrea AD. Fanconi anaemia forges a novel pathway. Nature Genet 1996; 14: 240-2.
-
(1996)
Nature Genet
, vol.14
, pp. 240-242
-
-
D'Andrea, A.D.1
-
19
-
-
0000436271
-
Complementation studies in Fanconi anemia
-
Schroeder-Kurt TM, Auerbach AD, Obe G (eds). Berlin, Heidelberg: Springer Verlag
-
Auerbach AD, Korse RE, Ghosh R, Venkatraj VS, Zhang M, Chiorazzi N. Complementation studies in Fanconi anemia. In: Schroeder-Kurt TM, Auerbach AD, Obe G (eds). Fanconi anemia, clinical, cytogenetic and experimental aspects. Berlin, Heidelberg: Springer Verlag, 1989: 213-25.
-
(1989)
Fanconi Anemia, Clinical, Cytogenetic and Experimental Aspects
, pp. 213-225
-
-
Auerbach, A.D.1
Korse, R.E.2
Ghosh, R.3
Venkatraj, V.S.4
Zhang, M.5
Chiorazzi, N.6
-
21
-
-
0026878842
-
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
-
Strathdee CA, Duncan AMV, Buchwald M. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nature Genet 1992; 1: 196-8.
-
(1992)
Nature Genet
, vol.1
, pp. 196-198
-
-
Strathdee, C.A.1
Duncan, A.M.V.2
Buchwald, M.3
-
22
-
-
0029163523
-
Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype
-
Joenje H, Lo Ten Foe JR, Oostra AB, van Berkel CGM, Rooimans MA, Schroeder-Kurt T et al. Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype. Blood 1995; 86 (12): 2156-60.
-
(1995)
Blood
, vol.86
, Issue.12
, pp. 2156-2160
-
-
Joenje, H.1
Lo Ten Foe, J.R.2
Oostra, A.B.3
Van Berkel, C.G.M.4
Rooimans, M.A.5
Schroeder-Kurt, T.6
-
23
-
-
84889179908
-
Fanconi anaemia in Europe
-
Müller HJ, Scott RJ, Webwer W (eds). Basel: Kavger
-
Joenje H, Lo Ten Foe JR, Oostra AB, Van Berkel CGM, di Summa F, Pronk JC. Fanconi anaemia in Europe. In: Müller HJ, Scott RJ, Webwer W (eds). Hereditary cancer. Basel: Kavger, 1995: 141-5.
-
(1995)
Hereditary Cancer
, pp. 141-145
-
-
Joenje, H.1
Lo Ten Foe, J.R.2
Oostra, A.B.3
Van Berkel, C.G.M.4
Di Summa, F.5
Pronk, J.C.6
-
24
-
-
0030023770
-
Fanconi anaemia complementation groups in Germany and the Netherlands
-
Joenje H. Fanconi anaemia complementation groups in Germany and The Netherlands. Hum Genet 1996; 97: 280-2.
-
(1996)
Hum Genet
, vol.97
, pp. 280-282
-
-
Joenje, H.1
-
25
-
-
16944362011
-
Evidence for at least eight Fanconi anemia genes
-
Joenje H, Oostra AB, van Berkel CGM, Di Summa F, Pronk JC, Arwert F. Evidence for at least eight Fanconi anemia genes. Am J Hum Genet 1997; 61: 940-4.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 940-944
-
-
Joenje, H.1
Oostra, A.B.2
Van Berkel, C.G.M.3
Di Summa, F.4
Pronk, J.C.5
Arwert, F.6
-
26
-
-
0026607986
-
Fanconi anemia. Current Concepts
-
Alter BR Fanconi anemia. Current Concepts. Am J Pediatr Hematol Oncol 1992; 14: 170-6.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 170-176
-
-
Alter, B.R.1
-
27
-
-
0029988091
-
Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity
-
Yamashita T, Wu N, Kupfer G, Corless C, Joenje H, Grompe M et al. Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity. Blood 1996; 87 (10): 4424-32.
-
(1996)
Blood
, vol.87
, Issue.10
, pp. 4424-4432
-
-
Yamashita, T.1
Wu, N.2
Kupfer, G.3
Corless, C.4
Joenje, H.5
Grompe, M.6
-
28
-
-
0024543636
-
International Fanconi Anemia Registry: Relation of clinical symptoms to diepoxibutane sensitivity
-
Auerbach AD, Rogatko A, Schroeder-Kurt TM. International Fanconi Anemia Registry: Relation of clinical symptoms to diepoxibutane sensitivity. Blood 1989; 73 (2): 391-6.
-
(1989)
Blood
, vol.73
, Issue.2
, pp. 391-396
-
-
Auerbach, A.D.1
Rogatko, A.2
Schroeder-Kurt, T.M.3
-
29
-
-
0029947378
-
Fanconi anaemia in Italy: High prevalence of complementation group A in two geographic clusters
-
Savoia A, Zatterale A, Del Principe D, Joenje H. Fanconi anaemia in Italy: High prevalence of complementation group A in two geographic clusters. Hum Genet 1996; 97: 599-603.
-
(1996)
Hum Genet
, vol.97
, pp. 599-603
-
-
Savoia, A.1
Zatterale, A.2
Del Principe, D.3
Joenje, H.4
-
31
-
-
0030197584
-
Molecular analysis of Fanconi anemia
-
Digweed M, Sperling K. Molecular analysis of Fanconi anemia. Bioessays 1996; 18: 5775-80.
-
(1996)
Bioessays
, vol.18
, pp. 5775-5780
-
-
Digweed, M.1
Sperling, K.2
-
32
-
-
0029835326
-
Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure
-
Jakobs PM, Sahaayaruban P, Saito H, Reifsteck C, Olson S, Joenje H et al. Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure. Somat Cell Mol Genet 1996; 22: 151-7.
-
(1996)
Somat Cell Mol Genet
, vol.22
, pp. 151-157
-
-
Jakobs, P.M.1
Sahaayaruban, P.2
Saito, H.3
Reifsteck, C.4
Olson, S.5
Joenje, H.6
-
33
-
-
84889229345
-
Significance of cellular sensitivity in a group of parents of Fanconi Anemia patients
-
Schroeder-Kurt TM, Auerbach AD, Obe G (eds). Berlin Heidelberg: Springer Verlag
-
Marx MP, Smith S. Significance of cellular sensitivity in a group of parents of Fanconi Anemia patients. In: Schroeder-Kurt TM, Auerbach AD, Obe G (eds). Fanconi anemia, clinical, cytogenetic and experimental aspects. Berlin Heidelberg: Springer Verlag, 1989: 425-33.
-
(1989)
Fanconi Anemia, Clinical, Cytogenetic and Experimental Aspects
, pp. 425-433
-
-
Marx, M.P.1
Smith, S.2
-
34
-
-
84889233555
-
Fanconi anemia in the Netherlans
-
Schroeder-Kurt TM, Auerbach AD, Obe G (eds). Berlin Heidelberg: Springer Verlag
-
Kwee ML, Kuyt LP. Fanconi anemia in the Netherlans. In: Schroeder-Kurt TM, Auerbach AD, Obe G (eds). Fanconi anemia, clinical, cytogenetic and experimental aspects. Berlin Heidelberg: Springer Verlag, 1989; 219-34.
-
(1989)
Fanconi Anemia, Clinical, Cytogenetic and Experimental Aspects
, pp. 219-234
-
-
Kwee, M.L.1
Kuyt, L.P.2
-
35
-
-
0029861118
-
Fanconi's anemia and malignancies
-
Alter BR Fanconi's anemia and malignancies. Am J Hematol 1996; 53: 99-110.
-
(1996)
Am J Hematol
, vol.53
, pp. 99-110
-
-
Alter, B.R.1
-
36
-
-
0026742503
-
VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies
-
Porteous MEM, Cross Y, Burn J. VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies. Am J Med Genet 1992; 43: 1032-5.
-
(1992)
Am J Med Genet
, vol.43
, pp. 1032-1035
-
-
Porteous, M.E.M.1
Cross, Y.2
Burn, J.3
-
37
-
-
0030039981
-
Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome
-
Rossbach HC, Sutcliffe MJ, Haag MM, Grana NH, Rossi AR, Barbosa JL. Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome. Am J Med Genet 1996; 61: 65-70.
-
(1996)
Am J Med Genet
, vol.61
, pp. 65-70
-
-
Rossbach, H.C.1
Sutcliffe, M.J.2
Haag, M.M.3
Grana, N.H.4
Rossi, A.R.5
Barbosa, J.L.6
-
38
-
-
1842326195
-
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience
-
Altay C, Alikasifoglu M, Kara A, Tuncbilek E, Ozbek N, Schroeder-Kurt TM. Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience. Clin Genet 1997; 51: 296-302.
-
(1997)
Clin Genet
, vol.51
, pp. 296-302
-
-
Altay, C.1
Alikasifoglu, M.2
Kara, A.3
Tuncbilek, E.4
Ozbek, N.5
Schroeder-Kurt, T.M.6
-
39
-
-
0028067640
-
Comparative study of Fanconi anaemia in children of different ethnic origin in South Africa
-
Macdougall LG, Rosendorff J, Poole JE, Cohn RJ, McElligott SE. Comparative study of Fanconi anaemia in children of different ethnic origin in South Africa. Am J Med Genet 1994; 52: 279-84.
-
(1994)
Am J Med Genet
, vol.52
, pp. 279-284
-
-
Macdougall, L.G.1
Rosendorff, J.2
Poole, J.E.3
Cohn, R.J.4
McElligott, S.E.5
-
40
-
-
12644293813
-
Somatic mosaicism in Fanconi anemia: Molecular Basis and clinical significance
-
Lo Ten Foe J, Rooimans MA, Guille JJP, Pals G, Kruyt FAE, Pronk J et al. Somatic mosaicism in Fanconi anemia: Molecular Basis and clinical significance. Eur J Hum Genet 1997; 5: 137-43.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 137-143
-
-
Lo Ten Foe, J.1
Rooimans, M.A.2
Guille, J.J.P.3
Pals, G.4
Kruyt, F.A.E.5
Pronk, J.6
-
41
-
-
0030882941
-
Identical mutations and phenotypic variation
-
Wolf U. Identical mutations and phenotypic variation. Hum Genet 1997; 100: 305-19.
-
(1997)
Hum Genet
, vol.100
, pp. 305-319
-
-
Wolf, U.1
|