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Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene

Indian journal of hematology & blood transfusion, 2016-03, Vol.32 (1), p.114-119

2016

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Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population

American journal of human biology, 2015-09, Vol.27 (5), p.716-719

2015

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Two new beta super(+)-thalassemia mutation [ beta -56 (G arrow right C); HBBc. -106 G arrow right C] and [ beta -83 (G arrow right A); HBBc. -133 G arrow right A] described among the Tunisian population

American journal of human biology, 2015-09, Vol.27 (5), p.716-719

2015

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Two new [beta]+-thalassemia mutation [[beta] -56 (G [arrow right] C); HBBc. -106 G [arrow right] C] and [[beta] -83 (G [arrow right] A); HBBc. -133 G [arrow right] A] described among the Tunisian population

American journal of human biology, 2015-09, Vol.27 (5), p.716

2015

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A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

Hemoglobin, 2014, Vol.38 (2), p.88-90

2014

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A New δ Chain Variant, Hb A 2 -Tunis [δ46(CD5)Gly → Glu; HBD : c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB : c.19G>A] β 0 -Thalassemia [IVS-I-1 (β143, G>A); HBB : c.92+1G>A]

Hemoglobin, 2014-04, Vol.38 (2), p.88-90

2014

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A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

Hemoglobin, 2014-04, Vol.38 (2), p.88-90

2014

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Haplotype Map of Sickle Cell Anemia in Tunisia

Disease markers, 2014-01, Vol.2014, p.938301-7

2014

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Restriction mapping of [beta]S locus among tunisian sickle-cell patients

American journal of human biology, 2011-11, Vol.23 (6), p.815

2011

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Restriction mapping of βS locus among tunisian sickle-cell patients

American journal of human biology, 2011-11, Vol.23 (6), p.815-819

2011

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Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian βS Chromosomes

Hemoglobin, 2012-08, Vol.36 (6), p.533-544

2012

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Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian β(S) Chromosomes

Hemoglobin, 2012-01

2012

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Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation

Hemoglobin, 2007-01, Vol.31 (1), p.23-29

2007

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Molecular basis of Hb H disease in southwest Iran

Hemoglobin, 2005, Vol.29 (1), p.43-50

2005

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Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) 0-Thalassemia Mutation

Hemoglobin, 2007, Vol.31 (1), p.23-29

2007

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Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation

Hemoglobin, 2007, Vol.31 (1), p.23-29

2007

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Hb A 2 -Pasteur-Tunis [δ59(E3)Lys→Asn, AA G →AA C ]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β 0 -Thalassemia Mutation

Hemoglobin, 2007-01, Vol.31 (1), p.23-29

2007

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Molecular Basis of Hb H Disease in Southwest Iran

Hemoglobin, 2005, Vol.29 (1), p.43-50

2005

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Rare thalassemic syndrome caused by interaction of Hb Questembert (α1 codon 131, TCT>CCT, Ser>Pro) with an α-thalassemia-2 deletion: implications for diagnosis and management

Blood cells, molecules, & diseases, 2004-01, Vol.32 (1), p.118-123

2004

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MOLECULAR SPECTRUM OF α-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH

Hemoglobin, 2002-01, Vol.26 (4), p.353-362

2002

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Hb H Disease Among Tunisians: Molecular Characterization of α-Thalassemia Determinants and Hematological Findings

Hemoglobin, 2003-01, Vol.27 (1), p.57-61

2003

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Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the [beta]-Globin Gene

Indian journal of hematology & blood transfusion, 2016-03, Vol.32 (1), p.114

2016

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Frequency and spectrum of hemochromatosis mutations in Tunisia

The hematology journal : the official journal of the European Haematology Association, 2003, Vol.4 (6), p.433

2003

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Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene

Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population

Two new beta super(+)-thalassemia mutation [ beta -56 (G arrow right C); HBBc. -106 G arrow right C] and [ beta -83 (G arrow right A); HBBc. -133 G arrow right A] described among the Tunisian population

Two new [beta]+-thalassemia mutation [[beta] -56 (G [arrow right] C); HBBc. -106 G [arrow right] C] and [[beta] -83 (G [arrow right] A); HBBc. -133 G [arrow right] A] described among the Tunisian population

A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

A New δ Chain Variant, Hb A 2 -Tunis [δ46(CD5)Gly → Glu; HBD : c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB : c.19G>A] β 0 -Thalassemia [IVS-I-1 (β143, G>A); HBB : c.92+1G>A]

A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]

Haplotype Map of Sickle Cell Anemia in Tunisia

Restriction mapping of [beta]S locus among tunisian sickle-cell patients

Restriction mapping of βS locus among tunisian sickle-cell patients

Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian βS Chromosomes

Microsatellite and Single Nucleotide Polymorphisms in the β-Globin Locus Control Region-Hypersensitive Site 2: Specificity of Tunisian β(S) Chromosomes

Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation

Molecular basis of Hb H disease in southwest Iran

Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) 0-Thalassemia Mutation

Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation

Hb A 2 -Pasteur-Tunis [δ59(E3)Lys→Asn, AA G →AA C ]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β 0 -Thalassemia Mutation

Molecular Basis of Hb H Disease in Southwest Iran

Rare thalassemic syndrome caused by interaction of Hb Questembert (α1 codon 131, TCT>CCT, Ser>Pro) with an α-thalassemia-2 deletion: implications for diagnosis and management

MOLECULAR SPECTRUM OF α-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH

Hb H Disease Among Tunisians: Molecular Characterization of α-Thalassemia Determinants and Hematological Findings

Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the [beta]-Globin Gene

Frequency and spectrum of hemochromatosis mutations in Tunisia

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