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Volumn 30, Issue 12, 2008, Pages 896-899

Significance of fetal hemoglobin values in detection of heterozygotes in fanconi anemia: Reevaluation of fetal hemoglobin values by a sensitive method

Author keywords

Carrier detection; Children; Fanconi anemia; Hb F; HPLC

Indexed keywords

HEMOGLOBIN F;

EID: 59149102063     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0b013e3181833835     Document Type: Article
Times cited : (6)

References (20)
  • 1
    • 1942509437 scopus 로고    scopus 로고
    • 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
  • 2
    • 0017136047 scopus 로고
    • Formal genetics of Fanconi's anemia
    • Schroeder TM, Tilgen D, Kruger J, et al. Formal genetics of Fanconi's anemia. Hum Genet. 1976;32:257-288.
    • (1976) Hum Genet , vol.32 , pp. 257-288
    • Schroeder, T.M.1    Tilgen, D.2    Kruger, J.3
  • 3
    • 0015216178 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.