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Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region

Haematologica (Roma), 2015-05, Vol.100 (5), p.e166

2015

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Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia

Hemoglobin, 2024-03, Vol.48 (2), p.116-117

2024

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Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-Thalassemia

Hemoglobin, 2024-03, Vol.48 (2), p.116-117

2024

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James Stewart (1934-2013)

Saothar (Dublin), 2014-01, Vol.39, p.125-125

Walker, Lynda

2014

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Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia

Hemoglobin, 2024-02, p.1

2024

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Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)

Hemoglobin, 2024-03, Vol.48 (2), p.113-115

2024

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β0-Thalassemia Caused by a Novel Nonsense Mutation [HBB:c.199A > T]

Hemoglobin, 2024-01, Vol.48 (1), p.69-70

2024

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β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]

Hemoglobin, 2024-01, Vol.48 (1), p.69-70

2024

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Incentive compensation: Bridging theory and practice

The Journal of Corporate Accounting & Finance, 2008-03, Vol.19 (3), p.35-40

2008

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Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene

Hemoglobin, 2017-11, Vol.41 (4-6), p.239-242

2017

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Experimental budgeting research: Implications for practitioners

The Journal of Corporate Accounting & Finance, 2007-09, Vol.18 (6), p.67-75

2007

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Compound Heterozygosity for Hb S and a Novel Deletion of Dnase I Hypersensitivity Sites HS3 and HS4 of β-Globin Locus Control Region Results in Hb S/β+-Thalassemia Phenotype

Blood, 2014-12, Vol.124 (21), p.2692-2692

2014

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α 0 -Thalassemia Due to a 90.7 kb Deletion (- - NFLD )

Hemoglobin, 2017-05, Vol.41 (3), p.218-219

2017

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α0-Thalassemia Due to a 90.7 kb Deletion (- -NFLD)

Hemoglobin, 2017-05, Vol.41 (3), p.218-219

2017

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Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)

Hemoglobin, 2016-09, Vol.40 (5), p.369-370

2016

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α + -Thalassemia Due to a Frameshift Mutation of the α 2-Globin Gene [codons 55/56 (+T) or HBA2 : c.168dup]

Hemoglobin, 2015-06, Vol.39 (3), p.209-210

2015

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α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]

Hemoglobin, 2012-04, Vol.36 (2), p.205-207

2012

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Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion

Hemoglobin, 2015-09, Vol.39 (5), p.368-370

2015

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Normal Hb A 2 β-Thalassemia Trait: Frameshift Mutation ( HBB : c.187_251dup) in Cis with the Hb A 2’ δ-Globin Gene Missense Mutation ( HBD : c.49G>C)

Hemoglobin, 2013-04, Vol.37 (2), p.201-204

2013

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α+-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup]

Hemoglobin, 2015, Vol.39 (3), p.209-210

2015

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Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of the β-Globin Gene Promoter (HBB: c.-133G > A)

Hemoglobin, 2014-12, Vol.38 (6), p.447-448

2014

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α+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG)

Hemoglobin, 2009-01, Vol.33 (1), p.72-74

2009

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Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2' δ-Globin Gene Missense Mutation (HBD: c.49G>C)

Hemoglobin, 2013, Vol.37 (2), p.201-204

2013

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Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)

Hemoglobin, 2013-01, Vol.37 (4), p.378-386

2013

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Repeatability of standardised nasal nitric oxide measurements in healthy and asthmatic adults and children

Respiratory medicine, 2005-09, Vol.99 (9), p.1105-1114

2005

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Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region

Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia

Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-Thalassemia

James Stewart (1934-2013)

Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia

Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)

β0-Thalassemia Caused by a Novel Nonsense Mutation [HBB:c.199A > T]

β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]

Incentive compensation: Bridging theory and practice

Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene

Experimental budgeting research: Implications for practitioners

Compound Heterozygosity for Hb S and a Novel Deletion of Dnase I Hypersensitivity Sites HS3 and HS4 of β-Globin Locus Control Region Results in Hb S/β+-Thalassemia Phenotype

α 0 -Thalassemia Due to a 90.7 kb Deletion (- - NFLD )

α0-Thalassemia Due to a 90.7 kb Deletion (- -NFLD)

Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)

α + -Thalassemia Due to a Frameshift Mutation of the α 2-Globin Gene [codons 55/56 (+T) or HBA2 : c.168dup]

α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]

Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion

Normal Hb A 2 β-Thalassemia Trait: Frameshift Mutation ( HBB : c.187_251dup) in Cis with the Hb A 2’ δ-Globin Gene Missense Mutation ( HBD : c.49G>C)

α+-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup]

Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of the β-Globin Gene Promoter (HBB: c.-133G > A)

α+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG)

Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2' δ-Globin Gene Missense Mutation (HBD: c.49G>C)

Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)

Repeatability of standardised nasal nitric oxide measurements in healthy and asthmatic adults and children

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