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Volumn 91, Issue 3, 2006, Pages 409-410

Hematologic and molecular characterization of a Sicilian cohort of α thalassemia carriers

Author keywords

thalassemia; globin genes; DHPLC; Non deletional mutations

Indexed keywords

ALPHA GLOBIN;

EID: 33645460312     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (9)
  • 2
    • 0036190154 scopus 로고    scopus 로고
    • HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
    • Hardison RC, Chui DH, Giardine B, Riemer C, Patrinos GP, Anagnou N, et al. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat 2002;19:225-33 http://globin.cse.psu.edu.
    • (2002) Hum Mutat , vol.19 , pp. 225-233
    • Hardison, R.C.1    Chui, D.H.2    Giardine, B.3    Riemer, C.4    Patrinos, G.P.5    Anagnou, N.6
  • 3
    • 0033900308 scopus 로고    scopus 로고
    • Laboratory investigation or hemoglobinopathies and thalassemias: Review and update
    • Clarke GM, Higgins TN. Laboratory investigation or hemoglobinopathies and thalassemias: review and update. Clin Chem 2000;46:1284-90.
    • (2000) Clin Chem , vol.46 , pp. 1284-1290
    • Clarke, G.M.1    Higgins, T.N.2
  • 4
    • 0037365343 scopus 로고    scopus 로고
    • Screening and genetic diagnosis of haemoglobin disorders
    • Old JM. Screening and genetic diagnosis of haemoglobin disorders. Blood Rev 2003;17:43-53.
    • (2003) Blood Rev , vol.17 , pp. 43-53
    • Old, J.M.1
  • 5
    • 27644467092 scopus 로고    scopus 로고
    • Molecular diagnosis of inherited disorders: Lessons from hemoglobinopathies
    • Patrinos GP, Kollia P, Papadakis MN. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies. Hum Mutat 2005;26:399-412.
    • (2005) Hum Mutat , vol.26 , pp. 399-412
    • Patrinos, G.P.1    Kollia, P.2    Papadakis, M.N.3
  • 6
    • 3042569513 scopus 로고    scopus 로고
    • Denaturing HPLC-based assay for molecular screening of nondeletional mutations causing α-thalassemias
    • Guida V, Colosimo A, Fiorito M, Foglietta E, Bianco I, Ivaldi G, et al. Denaturing HPLC-based assay for molecular screening of nondeletional mutations causing α-thalassemias. Clin Chem 2004;50:1242-5.
    • (2004) Clin Chem , vol.50 , pp. 1242-1245
    • Guida, V.1    Colosimo, A.2    Fiorito, M.3    Foglietta, E.4    Bianco, I.5    Ivaldi, G.6
  • 7
    • 0242330213 scopus 로고    scopus 로고
    • Rapid detection of six common Mediterranean and three non-Mediterranean α-thalassemia point mutations by reverse dot blot analysis
    • Foglietta E, Bianco I, Maggio A, Giambona A. Rapid detection of six common Mediterranean and three non-Mediterranean α-thalassemia point mutations by reverse dot blot analysis. Am J Hematol 2003;74:191-5.
    • (2003) Am J Hematol , vol.74 , pp. 191-195
    • Foglietta, E.1    Bianco, I.2    Maggio, A.3    Giambona, A.4
  • 8
    • 5044231544 scopus 로고    scopus 로고
    • Sequence variations of the α-globin genes: Scanning of high CG content genes with DHPLC and DG-DGGE
    • Lacerra G, Fiorito M, Musollino G, Di Noce F, Esposito M, Nigro V, et al. Sequence variations of the α-globin genes: scanning of high CG content genes with DHPLC and DG-DGGE. Hum Mutat 2004;24:338-49.
    • (2004) Hum Mutat , vol.24 , pp. 338-349
    • Lacerra, G.1    Fiorito, M.2    Musollino, G.3    Di Noce, F.4    Esposito, M.5    Nigro, V.6
  • 9
    • 0033792461 scopus 로고    scopus 로고
    • Diversity of α-globin mutations and clinical presentation of α-thalassemia in Israel
    • Oron-Kami V, Filon D, Shifrin Y, Fried E, Pogrebijsky G, Oppenheim A, et al. Diversity of α-globin mutations and clinical presentation of α-thalassemia in Israel. Am J Hematol 2000;65:196-203.
    • (2000) Am J Hematol , vol.65 , pp. 196-203
    • Oron-Kami, V.1    Filon, D.2    Shifrin, Y.3    Fried, E.4    Pogrebijsky, G.5    Oppenheim, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.