-
1
-
-
0013772684
-
Spontane Chromosomenaberrationen bei familiärer Panmyelopathie
-
Schroder TM, Anschütz F, Knopp A: Spontane Chromosomenaberrationen bei familiärer Panmyelopathie. Humangenetik 1964; 1: 194-196.
-
(1964)
Humangenetik
, vol.1
, pp. 194-196
-
-
Schroder, T.M.1
Anschütz, F.2
Knopp, A.3
-
2
-
-
0030197584
-
Molecular analysis of Fanconi anemia
-
Digweed M, Sperling K: Molecular analysis of Fanconi anemia . Bioessays 1996; 18: 579-585.
-
(1996)
Bioessays
, vol.18
, pp. 579-585
-
-
Digweed, M.1
Sperling, K.2
-
3
-
-
0002725969
-
Fanconi anemia
-
Vogelstein B, Kinzler KW (eds): McGraw-Hill: New York
-
Auerbach AD, Buchwald M, Joenje H: Fanconi anemia In Vogelstein B, Kinzler KW (eds): The Genetic Basis of Human Cancer McGraw-Hill: New York, 1998, pp 317-332.
-
(1998)
The Genetic Basis of Human Cancer
, pp. 317-332
-
-
Auerbach, A.D.1
Buchwald, M.2
Joenje, H.3
-
4
-
-
0018946141
-
Genetic heterogeneity of Franconi's anaemia demonstrated by somatic cell-hybrids
-
Zakrzewski S, Sperling K: Genetic heterogeneity of Franconi's anaemia demonstrated by somatic cell-hybrids. Hum Genet 1980; 56: 81-84.
-
(1980)
Hum Genet
, vol.56
, pp. 81-84
-
-
Zakrzewski, S.1
Sperling, K.2
-
5
-
-
16944362011
-
Evidence for at least eight Fanconi anemia genes
-
Joenje H, Oostra AB, Wijker M et al: Evidence for at least eight Fanconi anemia genes. Am J Hum Genet 1997; 61: 940-944.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 940-944
-
-
Joenje, H.1
Oostra, A.B.2
Wijker, M.3
-
6
-
-
0028840709
-
Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3
-
Pronk J, Gibson RA, Savoia A et al: Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3. Nat Genet 1995; 11: 338-340.
-
(1995)
Nat Genet
, vol.11
, pp. 338-340
-
-
Pronk, J.1
Gibson, R.A.2
Savoia, A.3
-
7
-
-
0026878842
-
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
-
Strathdee CA, Duncan AM, Buchwald M: Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nat Genet 1992; 1: 196-198.
-
(1992)
Nat Genet
, vol.1
, pp. 196-198
-
-
Strathdee, C.A.1
Duncan, A.M.2
Buchwald, M.3
-
8
-
-
0028857959
-
Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p
-
Whitney M, Thayer M, Reifsteck C et al: Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p. Nat Genet 1995; 11: 341-343.
-
(1995)
Nat Genet
, vol.11
, pp. 341-343
-
-
Whitney, M.1
Thayer, M.2
Reifsteck, C.3
-
9
-
-
0026521238
-
Cloning of cDNAs for Fanconi's anaemia by functional complementation
-
Strathde CA, Gavish H, Shannon WR, Buchwald M: Cloning of cDNAs for Fanconi's anaemia by functional complementation. Nature 1992; 356: 763-767.
-
(1992)
Nature
, vol.356
, pp. 763-767
-
-
Strathde, C.A.1
Gavish, H.2
Shannon, W.R.3
Buchwald, M.4
-
10
-
-
1842337370
-
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
-
Lo Ten Foe JR, Rooimans MA, Bosnoyan-Collins L et al: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA. Nat Genet 1996; 14: 320-323.
-
(1996)
Nat Genet
, vol.14
, pp. 320-323
-
-
Lo Ten Foe, J.R.1
Rooimans, M.A.2
Bosnoyan-Collins, L.3
-
11
-
-
0030293337
-
Positional cloning of the Fanconi anaemia group A gene
-
The Fanconi anaemia/Breast cancer consortium. Positional cloning of the Fanconi anaemia group A gene. Nat Genet 1996; 14: 324-328.
-
(1996)
Nat Genet
, vol.14
, pp. 324-328
-
-
-
12
-
-
0030667925
-
The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex
-
Kupfer GM, Naf D, Suliman D, Pulsipher M, D'Andrea AD: The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex. Nat Genet 1997; 17: 487-190.
-
(1997)
Nat Genet
, vol.17
, pp. 487-1190
-
-
Kupfer, G.M.1
Naf, D.2
Suliman, D.3
Pulsipher, M.4
D'Andrea, A.D.5
-
13
-
-
0030831350
-
The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2
-
Kupfer GM, Yamashita T, Naf D, Suliman A, Asano S, D'Andrea AD: The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2. Blood 1997; 90: 1047-1054.
-
(1997)
Blood
, vol.90
, pp. 1047-1054
-
-
Kupfer, G.M.1
Yamashita, T.2
Naf, D.3
Suliman, A.4
Asano, S.5
D'Andrea, A.D.6
-
14
-
-
0028938554
-
Irreversible repression of DNA synthesis in Fanconi anaemia cells is alleviated by the product of a novel cyclin-related gene
-
Digweed M, Günthert U, Schneider R, Seyschab H, Friedl R, Sperling K: Irreversible repression of DNA synthesis in Fanconi anaemia cells is alleviated by the product of a novel cyclin-related gene. Mol Cell Biol 1995; 15: 305-314.
-
(1995)
Mol Cell Biol
, vol.15
, pp. 305-314
-
-
Digweed, M.1
Günthert, U.2
Schneider, R.3
Seyschab, H.4
Friedl, R.5
Sperling, K.6
-
15
-
-
0030974684
-
Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase
-
Kruyt FA, Dijkmans LM, Arwert F, Joenje H: Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase. Cancer Res 1997; 57: 2244-2251.
-
(1997)
Cancer Res
, vol.57
, pp. 2244-2251
-
-
Kruyt, F.A.1
Dijkmans, L.M.2
Arwert, F.3
Joenje, H.4
-
16
-
-
0030023770
-
Fanconi anemia complementation groups in Germany and the Netherlands
-
Joenje H: Fanconi anemia complementation groups in Germany and the Netherlands. Hum Genet 1995; 97: 280-282.
-
(1995)
Hum Genet
, vol.97
, pp. 280-282
-
-
Joenje, H.1
-
17
-
-
0029163523
-
Classification of Fanconi anemia patients by complementation analysis: Evidence for a fifth genetic subtype
-
Joenje H, Lo Ten Foe JR, Oostra AB et al: Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype. Blood 1995; 86: 2156-2160.
-
(1995)
Blood
, vol.86
, pp. 2156-2160
-
-
Joenje, H.1
Lo Ten Foe, J.R.2
Oostra, A.B.3
-
18
-
-
0030453695
-
Fanconi anemia complementation group E: Clinical and cytogenetic data of the first patient
-
Wegner RD, Henrichs I, Joenje H, Schroeder-Kurth TM: Fanconi anemia complementation group E: clinical and cytogenetic data of the first patient. Clin Genet 1996; 30: 479-482.
-
(1996)
Clin Genet
, vol.30
, pp. 479-482
-
-
Wegner, R.D.1
Henrichs, I.2
Joenje, H.3
Schroeder-Kurth, T.M.4
-
19
-
-
0027514838
-
Localisation of Friedrich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
-
Ben Hamida C, Doerflinger N, Belal S et al: Localisation of Friedrich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nat Genet 1993; 5: 195-200.
-
(1993)
Nat Genet
, vol.5
, pp. 195-200
-
-
Ben Hamida, C.1
Doerflinger, N.2
Belal, S.3
-
20
-
-
0023239442
-
Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children
-
Lander ES, Botstein D: Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. Science 1987; 236: 1567-1570.
-
(1987)
Science
, vol.236
, pp. 1567-1570
-
-
Lander, E.S.1
Botstein, D.2
-
21
-
-
0015216178
-
Fanconi's anaemia in the genetics of neoplasia
-
Swift M: Fanconi's anaemia in the genetics of neoplasia. Nature 1971; 230: 370-373.
-
(1971)
Nature
, vol.230
, pp. 370-373
-
-
Swift, M.1
-
22
-
-
19244364472
-
A locus for Fanconi anemia on 16q determined by homozygosity mapping
-
Gschwend M, Levran O, Kruglyak L et al: A locus for Fanconi anemia on 16q determined by homozygosity mapping. Am J Hum Genet 1996; 59: 377-384.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 377-384
-
-
Gschwend, M.1
Levran, O.2
Kruglyak, L.3
-
23
-
-
0343472016
-
Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996
-
Povey S, Attwood J, Chadwick B et al: Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996. Ann Hum Genet 1997; 61: 183-206.
-
(1997)
Ann Hum Genet
, vol.61
, pp. 183-206
-
-
Povey, S.1
Attwood, J.2
Chadwick, B.3
-
24
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C et al: A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996; 380: 152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
|