Hemoglobin, Volume 31, Issue 3 (2007)

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Hemoglobin, Volume 31, Issue 3 (2007)

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Original

Article
An Overview of Current Microarray-Based Human Globin Gene Mutation Detection Methods
Laura Cremonesi, Maurizio Ferrari, Piero C. Giordano, Cornelis L. Harteveld, Marina Kleanthous, Thessalia Papasavva, George P. Patrinos & Joanne Traeger-Synodinos
Pages: 289-311
Published online: 07 Jul 2009
AbstractforAn Overview of Current Microarray-Based Human Globin Gene Mutation Detection Methods | Full Text | References | PDF (2.2 MB)
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Article
Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion
Cornelis L. Harteveld, Florens G.A. Versteegh, Eduard H.G. van Leer, Jaap S. Starreveld, Peter J.M.J. Kok, Irene van Rooijen-Nijdam, Peter van Delft, Isabelle Zanella-Cleon, Michel Becchi, Henri Wajcman & Piero C. Giordano
Pages: 313-323
Published online: 07 Jul 2009
AbstractforHb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion | Full Text | References | PDF (540.2 KB)
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Article
Hb Zoetermeer: A New Mutation on the α2 Gene Inducing an Ala→Ser Substitution at Codon 21 is Possibly Associated with a Mild Thalassemic Phenotype
Cornelis L. Harteveld, Willem C.H. van Helden, George L. Boxma, Peter van Delft, Margaretha Bakker-Verweij, Henri Wajcman, Isabelle Zanella-Cleon, Michel Becchi & Piero C. Giordano
Pages: 325-332
Published online: 07 Jul 2009
AbstractforHb Zoetermeer: A New Mutation on the α2 Gene Inducing an Ala→Ser Substitution at Codon 21 is Possibly Associated with a Mild Thalassemic Phenotype | Full Text | References | PDF (442.1 KB)
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Article
Globin Chain Synthesis is a Useful Complementary Tool in the Differential Diagnosis of Thalassemias
Shohreh Khatami, Soghra Rouhi Dehboneh, Sedigheh Sadeghi, Roghieh Mirzazadeh, Parinaz Saeedi, Parastoo Bayat, Hossein Najmabadi, Sirous Zeinali, Mohammad Taghi Akbari, Mohammad Ardjmand & Aref Amirkhani
Pages: 333-341
Published online: 07 Jul 2009
AbstractforGlobin Chain Synthesis is a Useful Complementary Tool in the Differential Diagnosis of Thalassemias | Full Text | References | PDF (175.1 KB)
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Article
The Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran
Ali Asghar Kiani, Yousef Mortazavi, Sirous Zeinali & Yaghob Shirkhani
Pages: 343-349
Published online: 07 Jul 2009
AbstractforThe Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran | Full Text | References | PDF (70.3 KB)
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Article
Distribution of β-Thalassemia Mutations in the Northern Provinces of Iran
Pupak Derakhshandeh-Peykar, Haleh Akhavan-Niaki, Ahmad Tamaddoni, Shohreh Ghawidel-Parsa, Kourosh Holakouie Naieni, Manijeh Rahmani, Farbod Babrzadeh, Mohammad Dilmaghani-Zadeh & Dariush Daneshvar Farhud
Pages: 351-356
Published online: 07 Jul 2009
AbstractforDistribution of β-Thalassemia Mutations in the Northern Provinces of Iran | Full Text | References | PDF (72.6 KB)
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Article
Skin Iron Concentration: a Simple, Highly Sensitive Method for Iron Stores Evaluation in Thalassemia Patients
Ilham Youssry, Nabil A. Mohsen, Olfat G. Shaker, Ahmed El-Hennawy, Rania Fawzy, Nagwa M. Abu-Zeid & Amal El-Beshlawy
Pages: 357-365
Published online: 07 Jul 2009
AbstractforSkin Iron Concentration: a Simple, Highly Sensitive Method for Iron Stores Evaluation in Thalassemia Patients | Full Text | References | PDF (95.4 KB)
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Short Communication

Article
Hb Leeds [β56(D7)Gly→Cys]: A New Hemoglobin that Aggravates Anemia in a child with β0-Thalassemia Trait
Jonathan P. Williams, James H. Scrivens, Brian N. Green, Lisa M. Farrar & Michaela Sutcliffe
Pages: 367-373
Published online: 07 Jul 2009
AbstractforHb Leeds [β56(D7)Gly→Cys]: A New Hemoglobin that Aggravates Anemia in a child with β0-Thalassemia Trait | Full Text | References | PDF (385.7 KB)
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Article
Hb L'Aquila [β106(G8)Leu→Val, CTG→GTG]: A Novel Thalassemic Hemoglobin Variant
Antonio Amato, Maria Pia Cappabianca, Donatella Ponzini, Silvana Rinaldi, Paola Di Biagio, Enrica Foglietta, Paola Grisanti & Fabrizio Mastropietro
Pages: 375-378
Published online: 07 Jul 2009
AbstractforHb L'Aquila [β106(G8)Leu→Val, CTG→GTG]: A Novel Thalassemic Hemoglobin Variant | Full Text | References | PDF (180.3 KB)
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Article
Hb Alesha [β67(E11)Val→Met, GTG→ATG] in an Argentinean Girl
Silvia Eandi Eberle, Nélida I. Noguera, Gabriela Sciuccati, Mariana Bonduel, Lilian Díaz, Raquel Staciuk, Héctor M. Targovnik & Aurora Feliu-Torres
Pages: 379-382
Published online: 07 Jul 2009
AbstractforHb Alesha [β67(E11)Val→Met, GTG→ATG] in an Argentinean Girl | Full Text | References | PDF (61.4 KB)
  • 54 Views
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Article
Ringed Sideroblasts Found in a Girl Heterozygous for the Initiation Codon (ATG→AGG) β0-Thalassemia Mutation
In-sang Jeon & Ki Lyong Nam
Pages: 383-386
Published online: 07 Jul 2009
AbstractforRinged Sideroblasts Found in a Girl Heterozygous for the Initiation Codon (ATG→AGG) β0-Thalassemia Mutation | Full Text | References | PDF (115.4 KB)
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Article
Genetic Origin of Hb D-Los Angeles [β121(GH4)Glu→Gln, GAA→CAA] According to the β-Globin Gene Cluster Haplotypes
Erol Ö. Atalay, Ayfer Atalay, Emre Üstel, Sanem Yildiz, Onur Öztürk, Aylin Köseler & Anzel Bahadir
Pages: 387-391
Published online: 07 Jul 2009
AbstractforGenetic Origin of Hb D-Los Angeles [β121(GH4)Glu→Gln, GAA→CAA] According to the β-Globin Gene Cluster Haplotypes | Full Text | References | PDF (66.4 KB)
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Article
A New Insertion Mutation in the β-Globin Gene [Codons 45/46 (+A)] Resulting in a β-Thalassemia Minor Phenotype
Gilbert Cornut, Xiaoduan Weng, Louise Robin, Catherine Lavoie, Sylvain Marchand & Denis Soulières
Pages: 393-395
Published online: 07 Jul 2009
AbstractforA New Insertion Mutation in the β-Globin Gene [Codons 45/46 (+A)] Resulting in a β-Thalassemia Minor Phenotype | Full Text | References | PDF (345.4 KB)
  • 36 Views
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Article
A Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family
Can Liao, Qiong Feng, Jian Li, Yining Huang & Dongzhi Li
Pages: 397-400
Published online: 07 Jul 2009
AbstractforA Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family | Full Text | References | PDF (278 KB)
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