Hemoglobin, Volume 30, Issue 3 (2006)

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Hemoglobin, Volume 30, Issue 3 (2006)

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ORIGINAL ARTICLE

Article
Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype
Cornelis L. Harteveld, Florens G.A. Versteegh, Peter J.M.J. Kok, Irene H. van Rooijen-Nijdam, Peter van Delft & Piero C. Giordano
Pages: 349-354
Published online: 07 Jul 2009
AbstractforHb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype | Full Text | References | PDF (90.7 KB)
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Article
Inherited Hemoglobin Disorders in Guinea-Bissau, West Africa: A Population Study
Tania N. Masmas, May-Lill Garly, Ida M. Lisse, Amabelia Rodriques, Pia T. Petersen & Henrik Birgens
Pages: 355-364
Published online: 07 Jul 2009
AbstractforInherited Hemoglobin Disorders in Guinea-Bissau, West Africa: A Population Study | Full Text | References | PDF (110.3 KB)
  • 108 Views
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Article
Prenatal Diagnosis of β-Thalassemia by Reverse Dot-Blot Hybridization in Southern China
Dongzhi Li, Can Liao, Jian Li, Yining Huang, Xingmei Xie, Jiaxue Wei & Shaoqing Wu
Pages: 365-370
Published online: 07 Jul 2009
AbstractforPrenatal Diagnosis of β-Thalassemia by Reverse Dot-Blot Hybridization in Southern China | Full Text | References | PDF (99.1 KB)
  • 92 Views
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Article
Gγ −37 (A→T): A New Nondeletional Hereditary Persistence of Fetal Hemoglobin Determinant Associated with the Rare Codon 91 (+T) δ0-Thalassemia
Marelle J. Bouva, Cornelis L. Harteveld, Greet Bakker-Verweij, Peter van Delft & Piero C. Giordano
Pages: 371-377
Published online: 07 Jul 2009
AbstractforGγ −37 (A→T): A New Nondeletional Hereditary Persistence of Fetal Hemoglobin Determinant Associated with the Rare Codon 91 (+T) δ0-Thalassemia | Full Text | References | PDF (100.7 KB)
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SHORT COMMUNICATION

Article
Hb LA Coruña [β38(C4)Thr→Ile]: A New Hemoglobin Variant Leading to Familial Polycythemia
Paloma Ropero, Carlos Fernández-Lago, Ana Villegas, Marta Polo, Marta Mateo, Asunción Mora & Fernando A. González
Pages: 379-383
Published online: 07 Jul 2009
AbstractforHb LA Coruña [β38(C4)Thr→Ile]: A New Hemoglobin Variant Leading to Familial Polycythemia | Full Text | References | PDF (89.1 KB)
  • 75 Views
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Article
Surface Plasmon Resonance-Based Molecular Detection of Hb S [β6(A3)Glu→Val, GAG→GTG] at the Gene Level
Erol Ö. Atalay, Emre Üstel, Sanem Yildiz & Ayfer Atalay
Pages: 385-391
Published online: 07 Jul 2009
AbstractforSurface Plasmon Resonance-Based Molecular Detection of Hb S [β6(A3)Glu→Val, GAG→GTG] at the Gene Level | Full Text | References | PDF (103.9 KB)
  • 57 Views
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Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child
Sumitra Dash, Keiko Harano & Santosh Menon
Pages: 393-396
Published online: 07 Jul 2009
AbstractforHb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child | Full Text | References | PDF (64.1 KB)
  • 74 Views
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Molecular Diagnosis of a Case of Hb Phnom Penh [α117(GH5)Phe-I1e-α118(H1)Thr (α1)]
Rock Y.-Y. Leung, Edmond S.-K. Ma, Amy Y.-Y. Chan & Eudora Y.-D. Chow
Pages: 397-399
Published online: 07 Jul 2009
AbstractforMolecular Diagnosis of a Case of Hb Phnom Penh [α117(GH5)Phe-I1e-α118(H1)Thr (α1)] | Full Text | References | PDF (59.4 KB)
  • 175 Views
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Hb Southampton [β106(G8)Leu→Pro, CTG→CCG] in an Argentinean Boy
Silvia Eandi Eberle, Nélida I. Noguera, Gabriela Sciuccati, Mariana Bonduel, Lilian Díaz, Raquel Staciuk & Aurora Feliu-Torres
Pages: 401-403
Published online: 07 Jul 2009
AbstractforHb Southampton [β106(G8)Leu→Pro, CTG→CCG] in an Argentinean Boy | Full Text | References | PDF (53.5 KB)
  • 91 Views
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Detection of a Rare β-Globin Nonsense Mutation [Codon 59 (AAG→TAG)] in an Italian Family
Antonio Amato, Maria Pia Cappabianca, Donatella Ponzini, Paola Di Biagio, Alessia Colosimo, Valentina Guida, Fabrizio Mastropietro, Enrica Foglietta, Paola Grisanti, Silvana Rinaldi, Bruno Dallapiccola & Ida Bianco
Pages: 405-407
Published online: 07 Jul 2009
AbstractforDetection of a Rare β-Globin Nonsense Mutation [Codon 59 (AAG→TAG)] in an Italian Family | Full Text | References | PDF (61.2 KB)
  • 24 Views
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