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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 5-6
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Original Article

Biochemical and Molecular Aspects of β-Thalassemia Types in Northern Sardinia

B. Masala Institute of General Physiology and Biochemistry University of Sassari, Sassari, Italy
,
L. Manca Institute of General Physiology and Biochemistry University of Sassari, Sassari, Italy
,
D. Gallisai Institute and Clinic of Pediatrics University of Sassari, Sassari, Italy
,
A. Stangoni Transfusion and Immunohematology Service General Hospital, Sassari, Italy
,
K. D. Lanclos Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
F. Kutlar Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
K. G. Yang Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H. J. Huisnan Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
 show all
Pages 661-671 | Received 19 Oct 1987, Accepted 07 Jun 1988, Published online: 07 Jul 2009

Citations (11)

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Read on this site (1)

Bruno Masala. (1992) Hemoglobinopathies in Sardinia. Hemoglobin 16:4, pages 331-351.
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Articles from other publishers (10)

Laura Manca & Bruno Masala. (2008) Disorders of the synthesis of human fetal hemoglobin. IUBMB Life 60:2, pages 94-111.
Crossref
Ignazio Piras, Maria Elena Ghiani, Laurent Varesi, Carla Calo, Alessandra Falchi, Giuseppe Vona & Laurianne Giovannoni. (2006) Distribution of ݭGlobin Cluster Haplotypes in Sardinia (Italy). Distribution of ݭGlobin Cluster Haplotypes in Sardinia (Italy).
I. Piras, G. Vona, A. Falchi, V. Latini, S. Ristaldi, L. Vacca, L. Varesi & C.M. Calò*. (2005) β-globin cluster haplotypes in normal individuals and β039-thalassemia carriers from Sardinia, Italy. American Journal of Human Biology 17:6, pages 765-772.
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Alessandra Falchi, Laurianne Giovannoni, Lucia Vacca, Veronica Latini, Giuseppe Vona & Laurent Varesi. (2005) ?-globin gene cluster haplotypes associated with ?-thalassemia on Corsica island. American Journal of Hematology 78:1, pages 27-32.
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John G. Gilman, Laura Manca, Laura Frogheri, Paola Pistidda, Luciana Guiso, Maurizio Longinotti & Bruno Masala. (2006) Mild β + (−87)‐thalassemia CACCC box mutation is associated with elevated fetal hemoglobin expression in cis . American Journal of Hematology 45:3, pages 265-267.
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Bruno Masala & Laura Manca. 1994. Hemoglobins Part B: Biochemical and Analytical Methods. Hemoglobins Part B: Biochemical and Analytical Methods 21 44 .
L. Manca, E. Cocco, D. Gallisai, B. Masala & J. G. Gilman. (2008) Diminished A γ T fetal globin levels in Sardinian haplotype II β°‐thalassaemia patients are associated with a four base pair deletion in the A γ T promoter . British Journal of Haematology 78:1, pages 105-107.
Crossref
Bruno Masala & Laura Manca. (1991) Detection of the common Hb F Sardinia [Aγ(E19)Ile → Thr]variant by isoelectric focusing in normal newborns and in adults affected by elevated fetal hemoglobin syndromes. Clinica Chimica Acta 198:3, pages 195-202.
Crossref
L. MANCA, E. COCCO, D. GALLISAI, B. MASALA & J. G. GILMAN. (1990) Sardinian Haplotype II ? 0 -Thalassemia Is Linked to the Variant A ? T -Globin Gene with a 4-Bp Promoter Deletion and Diminished A ? T Expression b, . Annals of the New York Academy of Sciences 612:1 Sixth Cooley', pages 485-487.
Crossref
Bruno Masala & Laura Manca. (1990) High-performance liquid chromatography of globin chains in the identification of human globin gene abnormalities.. Biophysical Chemistry 37:1-3, pages 225-230.
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