Hemoglobin, Volume 36, Issue 2 (2012)

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Hemoglobin, Volume 36, Issue 2 (2012)

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Original Article

Article
Neonatal Cyanosis Due to A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Sarajevo [Gγ102(G4)Asn→Thr, AAC>ACC]
Urs Zimmermann-Baer, Ralph Capalo, Fabrizio Dutly, Elisabeth Saller, Heinz Troxler, Malcolm Kohler & Hannes Frischknecht
Pages: 109-113
Published online: 02 Mar 2012
AbstractforNeonatal Cyanosis Due to A New Gγ-Globin Variant Causing Low Oxygen Affinity: Hb F-Sarajevo [Gγ102(G4)Asn→Thr, AAC>ACC] | Full Text | References | PDF (235.5 KB)
  • 187 Views
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Article
Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?
Khushnooma Y. Italia, Pratibha M. Sawant, Anita H. Nadkarni, Kanjaksha Ghosh & Roshan B. Colah
Pages: 114-123
Published online: 01 Feb 2012
AbstractforIs the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography? | Full Text | References | PDF (391.5 KB)
  • 86 Views
  • 6 CrossRef citations
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Article
Simultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran
Haleh Akhavan-Niaki, Ali Banihashemi, Amrollah Mostafazadeh, Vahid Kholghi Oskooei, Mandana Azizi, Reza Youssefi Kamangar & Maryam Mitra Elmi
Pages: 124-130
Published online: 22 Feb 2012
AbstractforSimultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran | Full Text | References | PDF (1.1 MB)
  • 116 Views
  • 2 CrossRef citations
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Article
Prevalence and Molecular Analysis of β-Thalassemia in Adiyaman, Turkey
Ahmet Genc, Deniz Tastemir Korkmaz, Mehmet Buyukleyla & Murat Celiker
Pages: 131-138
Published online: 22 Feb 2012
AbstractforPrevalence and Molecular Analysis of β-Thalassemia in Adiyaman, Turkey | Full Text | References | PDF (329.3 KB)
  • 240 Views
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Article
α-Thalassemia Mutations in Two Provinces of Southern Iran: FARS & Kohkeloye and Bouyer Ahmad
Faramarzi Hossein, Rastegar Mohsen, Moghadami Mohsen & Mohammad Taheri
Pages: 139-143
Published online: 08 Mar 2012
Abstractforα-Thalassemia Mutations in Two Provinces of Southern Iran: FARS & Kohkeloye and Bouyer Ahmad | Full Text | References | PDF (130.3 KB)
  • 101 Views
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Short Communications

Article
Prenatal Diagnosis of Hemoglobinopathies by Pyrosequencing: A More Sensitive and Rapid Approach to Fetal Genotyping
Adele T. Timbs, Michelle J. Rugless, Alice E. Gallienne, Anna M. Haywood, Shirley J. Henderson & John M. Old
Pages: 144-150
Published online: 12 Jan 2012
AbstractforPrenatal Diagnosis of Hemoglobinopathies by Pyrosequencing: A More Sensitive and Rapid Approach to Fetal Genotyping | Full Text | References | PDF (260.6 KB)
  • 219 Views
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Article
A New β Chain Hemoglobin Variant With Increased Oxygen Affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G]
Antonella Fais, Maria Carla Sollaino, Susanna Barella, Lucia Perseu, Benedetta Era & Marcella Corda
Pages: 151-156
Published online: 04 Jan 2012
AbstractforA New β Chain Hemoglobin Variant With Increased Oxygen Affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G] | Full Text | References | PDF (272.3 KB)
  • 127 Views
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Article
Association of Hb New York with Hb E and α0-Thalassemia in a Chinese Woman Identified by Sebia Capillarys2 System
Dong-Zhi Li, Jian-Ying Zhou, Xing-Mei Xie & Can Liao
Pages: 157-160
Published online: 22 Feb 2012
AbstractforAssociation of Hb New York with Hb E and α0-Thalassemia in a Chinese Woman Identified by Sebia Capillarys2 System | Full Text | References | PDF (255.3 KB)
  • 127 Views
  • 1 CrossRef citations
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Article
A Case Report of a Male Patient With Hb Hammersmith [β42(CD1)Phe→Ser, TTT>TCT]
Seungman Park, Hyoung Jin Kang, Sung Im Cho, So Yeon Kim, Moon-Woo Seong & Sung Sup Park
Pages: 161-165
Published online: 04 Jan 2012
AbstractforA Case Report of a Male Patient With Hb Hammersmith [β42(CD1)Phe→Ser, TTT>TCT] | Full Text | References | PDF (173.9 KB)
  • 169 Views
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Article
Analysis of the rs35959442 Polymorphism in Hb E/β-Thalassemia in Guangxi Province of the Republic of China
Yunyan He, Ping Chen, Weixiong Lin & Jianming Luo
Pages: 166-169
Published online: 22 Dec 2011
AbstractforAnalysis of the rs35959442 Polymorphism in Hb E/β-Thalassemia in Guangxi Province of the Republic of China | Full Text | References | PDF (201.3 KB)
  • 115 Views
  • 2 CrossRef citations
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Article
Identification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region [+1,506 (A>C)] in a Japanese Male with a Heterozygous β-Thalassemia Phenotype
Minako Hino, Yasuhiro Yamashiro, Yukio Hattori, Hitomi Ito, Takenori Nitta, Chris Adhiyanto, Maryam Matar & Mohammed Naveed
Pages: 170-176
Published online: 04 Jan 2012
AbstractforIdentification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region [+1,506 (A>C)] in a Japanese Male with a Heterozygous β-Thalassemia Phenotype | Full Text | References | PDF (627.4 KB)
  • 157 Views
  • 8 CrossRef citations
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Article
Comparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels
Elisabeth Saller, Kamran Moradkhani, Fabrizio Dutly, Isabelle Vinatier, Claude Préhu, Hannes Frischknecht & Michel Goossens
Pages: 177-182
Published online: 24 Jan 2012
AbstractforComparison of Two Known Chromosomal Rearrangements in the δβ-Globin Complex with Identical DNA Breakpoints but Causing Different Hb A2 Levels | Full Text | References | PDF (136.2 KB)
  • 106 Views
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Article
Hyperhemolysis Syndrome Complicating Pregnancy in Homozygous δβ-Thalassemia
Joseph Mechery, Kehinde Abidogun, Fiona Crosfill & James Jip
Pages: 183-185
Published online: 12 Jan 2012
AbstractforHyperhemolysis Syndrome Complicating Pregnancy in Homozygous δβ-Thalassemia | Full Text | References | PDF (116.8 KB)
  • 182 Views
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Article
Cord Blood Analysis for Rapid Prenatal Confirmation of Hb Bart’s Disease Using the Sebia Capillary Electrophoresis System
Can Liao, Jian-Ying Zhou, Xing-Mei Xie, Ru Li & Dong-Zhi Li
Pages: 186-191
Published online: 22 Dec 2011
AbstractforCord Blood Analysis for Rapid Prenatal Confirmation of Hb Bart’s Disease Using the Sebia Capillary Electrophoresis System | Full Text | References | PDF (294 KB)
  • 142 Views
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Article
A Novel α-Thalassemia Frameshift Mutation: Codon 8 (–C)
Hai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, Ru Li, Can Liao & Dong-Zhi Li
Pages: 192-195
Published online: 13 Jan 2012
AbstractforA Novel α-Thalassemia Frameshift Mutation: Codon 8 (–C) | Full Text | References | PDF (353.2 KB)
  • 114 Views
  • 1 CrossRef citations
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Article
Screening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System
Hai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, Ru Li, Can Liao & Dong-Zhi Li
Pages: 196-199
Published online: 12 Jan 2012
AbstractforScreening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System | Full Text | References | PDF (130.4 KB)
  • 239 Views
  • 5 CrossRef citations
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Article
A Rare Hb H Disease Due to the – –SEA and 16.6 kb α-Thalassemia-2 Deletions
Suravee Sroymora, Sumalee Jindadamrongwech, Punnee Butthep & Suporn Chuncharunee
Pages: 200-204
Published online: 29 Feb 2012
AbstractforA Rare Hb H Disease Due to the – –SEA and 16.6 kb α-Thalassemia-2 Deletions | Full Text | References | PDF (339.5 KB)
  • 139 Views
  • 4 CrossRef citations
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Article
α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]
John S. Waye, Lynda Walker & Barry Eng
Pages: 205-207
Published online: 29 Feb 2012
Abstractforα+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT] | Full Text | References | PDF (181 KB)
  • 83 Views
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