-
1
-
-
1942509437
-
Inherited bone marrow failure syndromes
-
Nathan DG, Oski FA, eds, 6th ed. Philadelphia: WB Saunders;
-
Alter BP. Inherited bone marrow failure syndromes. In: Nathan DG, Oski FA, eds. Hematology of Infancy and Childhood. 6th ed. Philadelphia: WB Saunders; 2003:280-365.
-
(2003)
Hematology of Infancy and Childhood
, pp. 280-365
-
-
Alter, B.P.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
-
-
0023759650
-
Fanconi's anemia - chromosome breakage studies in homozygotes and heterozygotes
-
Rosendorff J, Bernstein R. Fanconi's anemia - chromosome breakage studies in homozygotes and heterozygotes. Cancer Genet Cytogenet. 1988;33:175-183.
-
(1988)
Cancer Genet Cytogenet
, vol.33
, pp. 175-183
-
-
Rosendorff, J.1
Bernstein, R.2
-
5
-
-
0028858123
-
Carrier frequency of the IVS4+4 A->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population
-
Verlander PC, Kaporis A, Liu Q, et al. Carrier frequency of the IVS4+4 A->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population. Blood. 1995;86:4034-4038.
-
(1995)
Blood
, vol.86
, pp. 4034-4038
-
-
Verlander, P.C.1
Kaporis, A.2
Liu, Q.3
-
6
-
-
1842326195
-
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience
-
Altay C, Alikasifoglu M, Kara A, et al. 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
-
7
-
-
0019974447
-
Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anemia, and xeroderma pigmentosum families
-
Welshimer K, Swift M. Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anemia, and xeroderma pigmentosum families. Am J Hum Genet. 1982; 34:781-793.
-
(1982)
Am J Hum Genet
, vol.34
, pp. 781-793
-
-
Welshimer, K.1
Swift, M.2
-
8
-
-
0016855511
-
Letter: Fanconi's anemia in offspring of patient with congenital radial and carpal hypoplasia
-
Altay C, Sevgi Y, Pirnar T. Letter: Fanconi's anemia in offspring of patient with congenital radial and carpal hypoplasia. N Engl J Med. 1975;293:151-152.
-
(1975)
N Engl J Med
, vol.293
, pp. 151-152
-
-
Altay, C.1
Sevgi, Y.2
Pirnar, T.3
-
9
-
-
0017883557
-
Fanconi's anaemia, with special reference to erythrokinetic features
-
Skikne BS, Lynch SR, Bezwoda WR, et al. Fanconi's anaemia, with special reference to erythrokinetic features. S Afr Med J. 1978; 53:43-50.
-
(1978)
S Afr Med J
, vol.53
, pp. 43-50
-
-
Skikne, B.S.1
Lynch, S.R.2
Bezwoda, W.R.3
-
10
-
-
0025006172
-
Physical and laboratory characteristics of heterozygote carriers of the Fanconi aplasia gene
-
Petridou M, Barrett 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
Barrett, A.J.2
-
11
-
-
0023522036
-
High-performance liquid chromatography as a method to identify haemoglobin abnormalities
-
Huisman TH. High-performance liquid chromatography as a method to identify haemoglobin abnormalities. Acta Haematol. 1987;78:123-126.
-
(1987)
Acta Haematol
, vol.78
, pp. 123-126
-
-
Huisman, T.H.1
-
12
-
-
0025302542
-
Fetal hemoglobin in normal adults and beta-thalassemia heterozygotes
-
Kutlar A, Kutlar F, Gu LG, et al. Fetal hemoglobin in normal adults and beta-thalassemia heterozygotes. Hum Genet. 1990; 85:106-110.
-
(1990)
Hum Genet
, vol.85
, pp. 106-110
-
-
Kutlar, A.1
Kutlar, F.2
Gu, L.G.3
-
13
-
-
0027486127
-
New ultra-micro high-performance liquid chromatographic method for determining the gamma chain composition of hemoglobin F in normal adults
-
Kutlar F, Huisman TH. New ultra-micro high-performance liquid chromatographic method for determining the gamma chain composition of hemoglobin F in normal adults. J Chromatogr. 1993;620:183-189.
-
(1993)
J Chromatogr
, vol.620
, pp. 183-189
-
-
Kutlar, F.1
Huisman, T.H.2
-
14
-
-
0031292855
-
Fanconi anemia: Genetic testing in Ashkenazi Jews
-
Auerbach AD. Fanconi anemia: genetic testing in Ashkenazi Jews. Genet Test. 1997;1:27-33.
-
(1997)
Genet Test
, vol.1
, pp. 27-33
-
-
Auerbach, A.D.1
-
15
-
-
0032898006
-
Heterogeneous spectrum of mutations in the Fanconi anemia group A gene
-
Wijker M, Morgan NV, Herterich S, et al. Heterogeneous spectrum of mutations in the Fanconi anemia group A gene. Eur J Hum Genet. 1999;7:52-59.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 52-59
-
-
Wijker, M.1
Morgan, N.V.2
Herterich, S.3
-
16
-
-
0022588993
-
Diabetes mellitus in ataxia-telangiectasia, Fanconi anemia, xeroderma pigmentosum, common variable immune deficiency, and severe combined immune deficiency families
-
Morrell D, Chase CL, Kupper LL, et al. Diabetes mellitus in ataxia-telangiectasia, Fanconi anemia, xeroderma pigmentosum, common variable immune deficiency, and severe combined immune deficiency families. Diabetes. 1986;35:143-147.
-
(1986)
Diabetes
, vol.35
, pp. 143-147
-
-
Morrell, D.1
Chase, C.L.2
Kupper, L.L.3
-
17
-
-
66249126693
-
Diseases of DNA repair
-
Kidson C. Diseases of DNA repair. Clin Haematol. 1980; 65:143-147.
-
(1980)
Clin Haematol
, vol.65
, pp. 143-147
-
-
Kidson, C.1
-
18
-
-
0017116304
-
Familial cancer on a Scottish island
-
Hill RD. Familial cancer on a Scottish island. Br Med J. 1976; 2:401-402.
-
(1976)
Br Med J
, vol.2
, pp. 401-402
-
-
Hill, R.D.1
-
19
-
-
0019200064
-
Reassessment of cancer predisposition of Fanconi anemia heterozygotes
-
Swift M, Caldwell RJ, Chase C. Reassessment of cancer predisposition of Fanconi anemia heterozygotes. J Natl Cancer Inst. 1980; 65:863-867.
-
(1980)
J Natl Cancer Inst
, vol.65
, pp. 863-867
-
-
Swift, M.1
Caldwell, R.J.2
Chase, C.3
-
20
-
-
0026751087
-
Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemia
-
Rosatelli MC, Altay C, Oner R, et al. Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemia. Haematologica. 1992;77: 106-109.
-
(1992)
Haematologica
, vol.77
, pp. 106-109
-
-
Rosatelli, M.C.1
Altay, C.2
Oner, R.3
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