-
1
-
-
0014112634
-
Familial constitutional panmyelocytopathy, Fanconi's anemia (FA). I. Clinical aspects
-
Fanconi G: Familial constitutional panmyelocytopathy, Fanconi's anemia (FA). I. Clinical aspects. Semin Hematol 1967;4:233-240.
-
(1967)
Semin Hematol
, vol.4
, pp. 233-240
-
-
Fanconi, G.1
-
3
-
-
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
-
4
-
-
0019378276
-
Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia
-
Cervenka J, Arthur D, Yasis C: Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia. Pediatrics 1981;67:119-127.
-
(1981)
Pediatrics
, vol.67
, pp. 119-127
-
-
Cervenka, J.1
Arthur, D.2
Yasis, C.3
-
5
-
-
0027861014
-
Fanconi anemia diagnosis and the diepoxybutane (DEB) test
-
Auerbach AD: Fanconi anemia diagnosis and the diepoxybutane (DEB) test. Exp Hematol 1993;21:731-733.
-
(1993)
Exp Hematol
, vol.21
, pp. 731-733
-
-
Auerbach, A.D.1
-
6
-
-
0020047791
-
Deficient natural killer cell activity in a patient with Fanconi's anemia and squamous cell carcinoma: Association with defect in interferon release
-
Hersey P, Edwards A, Lewis R, Kemp A, Mcinnes J: Deficient natural killer cell activity in a patient with Fanconi's anemia and squamous cell carcinoma: Association with defect in interferon release. Clin Exp Immunol 1982; 48:205-212.
-
(1982)
Clin Exp Immunol
, vol.48
, pp. 205-212
-
-
Hersey, P.1
Edwards, A.2
Lewis, R.3
Kemp, A.4
Mcinnes, J.5
-
7
-
-
0023129832
-
Reduced natural killer activity in patients with Fanconi's anemia and in family members
-
Froom P, Aghai E, Dobinsky JB, Quitt M, Lahat N: Reduced natural killer activity in patients with Fanconi's anemia and in family members. Leuk Res 1987;11:197-199.
-
(1987)
Leuk Res
, vol.11
, pp. 197-199
-
-
Froom, P.1
Aghai, E.2
Dobinsky, J.B.3
Quitt, M.4
Lahat, N.5
-
8
-
-
0021923167
-
Cytogenetic analyses utilizing various clastogens in two sibs with Fanconi anemia, their relatives and control individuals
-
Gebbart E, Kysela D, Matthes H, Nikol M: Cytogenetic analyses utilizing various clastogens in two sibs with Fanconi anemia, their relatives and control individuals. Hum Genet 1985;69:309-315.
-
(1985)
Hum Genet
, vol.69
, pp. 309-315
-
-
Gebbart, E.1
Kysela, D.2
Matthes, H.3
Nikol, M.4
-
9
-
-
0026547984
-
Abnormal lymphokine production: A novel feature of the genetic disease of Fanconi anemia
-
Rosselli F, Sanceau J, Wietzerbin J, Moustacchi E: Abnormal lymphokine production: A novel feature of the genetic disease of Fanconi anemia. Hum Genet 1992;89:42-48.
-
(1992)
Hum Genet
, vol.89
, pp. 42-48
-
-
Rosselli, F.1
Sanceau, J.2
Wietzerbin, J.3
Moustacchi, E.4
-
10
-
-
0028123475
-
Abnormal lymphokine production: A novel feature of the genetic disease of Fanconi anemia. II. In vitro and in vivo spontaneous overproduction of tumor necrosis factor α
-
Rosselli F, Sanceau J, Gluckman E, Wietzerbin J, Moustacchi E: Abnormal lymphokine production: A novel feature of the genetic disease of Fanconi anemia. II. In vitro and in vivo spontaneous overproduction of tumor necrosis factor α. Blood 1994;83:1216-1225.
-
(1994)
Blood
, vol.83
, pp. 1216-1225
-
-
Rosselli, F.1
Sanceau, J.2
Gluckman, E.3
Wietzerbin, J.4
Moustacchi, E.5
-
11
-
-
0027376655
-
Anomalous plasma concentration and impaired secretion of growth factors in Fanconi's anemia
-
Wunder E, Thing Mortensen B, Schilling F, Henon PR: Anomalous plasma concentration and impaired secretion of growth factors in Fanconi's anemia. Stem Cells 1993;11(suppl 2):144-149.
-
(1993)
Stem Cells
, vol.11
, Issue.2 SUPPL.
, pp. 144-149
-
-
Wunder, E.1
Thing Mortensen, B.2
Schilling, F.3
Henon, P.R.4
-
12
-
-
0019974447
-
Congenital malformations and developmental disabilities in ataxiatelangiectasia, Fanconi anemia, and xeroderma pigmentosum families
-
Weisheimer K, Swift M: Congenital malformations and developmental disabilities in ataxiatelangiectasia, Fanconi anemia, and xeroderma pigmentosum families. Am J Hum Genet 1982; 34:781-793.
-
(1982)
Am J Hum Genet
, vol.34
, pp. 781-793
-
-
Weisheimer, K.1
Swift, M.2
-
13
-
-
0005138257
-
Prenatal and postnatal diagnosis of aplastic anemia
-
Alter BP (ed): Edinburgh, Churchill Livingstone
-
Auerbach AD, Alter BP: Prenatal and postnatal diagnosis of aplastic anemia; in Alter BP (ed): Perinatal Hematology: Methods in Hematology Series. Edinburgh, Churchill Livingstone, 1989, pp 225-251.
-
(1989)
Perinatal Hematology: Methods in Hematology Series
, pp. 225-251
-
-
Auerbach, A.D.1
Alter, B.P.2
-
15
-
-
0025006172
-
Physical and laboratory characteristics of heterozygote carriers of the Fanconi aplasia gene
-
Petridou M, Barret AJ: Physical and laboratory characteristics of heterozygote carriers of the Fanconi aplasia gene. Acta Paediatr Scand 1990;79:1069-1074.
-
(1990)
Acta Paediatr Scand
, vol.79
, pp. 1069-1074
-
-
Petridou, M.1
Barret, A.J.2
-
17
-
-
0003565214
-
-
Berkeley, University of California Press
-
BMDP: Statistical Software Manual. Berkeley, University of California Press, 1992.
-
(1992)
Statistical Software Manual
-
-
|