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Novel 27.9 kb α 0 ‐thalassemia deletion in a Filipino woman

American journal of hematology, 2009-03, Vol.84 (3), p.197-198

2009

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Digging deeper into the limits of ancient DNA research on syphilis

Journal of archaeological science, 2007-12, Vol.34 (12), p.2091-2100

2007

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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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Novel 27.9 kb alpha(0)-thalassemia deletion in a Filipino woman

American journal of hematology, 2009-03, Vol.84 (3), p.197-198

2009

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Molecular Characterization of a Novel 55.1 kb Gγ(Aγδβ)0-thalassemia Deletion in Two Canadian Families

Hemoglobin, 2009-12, Vol.33 (6), p.422-427

2009

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Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC)

Hemoglobin, 2008-01, Vol.32 (3), p.315-317

2008

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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 Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T)

Hemoglobin, 2009-12, Vol.33 (6), p.519-522

2009

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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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Characterisation of a novel 49.3 kb Ggamma(Agamma delta beta)(0) -thalassaemia deletion in seven families of Asian descent

British journal of haematology, 2007-07, Vol.138 (1), p.125-126

2007

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Characterisation of a novel 49·3 kb Gγ(Aγδβ)0‐thalassaemia deletion in seven families of Asian descent

British journal of haematology, 2007-07, Vol.138 (1), p.125-126

2007

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Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC)

Hemoglobin, 2008, Vol.32 (3), p.315-317

2008

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Improved DNA extraction from ancient bones using silica-based spin columns

American journal of physical anthropology, 1998-04, Vol.105 (4), p.539-543

1998

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Evaluation of the CapillaryS 2 CE System for Hemoglobinopathy Investigations

Blood, 2006-11, Vol.108 (11), p.3781-3781

2006

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Hb H hydrops foetalis syndrome: a case report and review of literature

British journal of haematology, 2001-10, Vol.115 (1), p.72-78

2001

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Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutations

Developmental medicine and child neurology, 2006-05, Vol.48 (5), p.383-387

2006

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Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG)

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

2009

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Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families

Hemoglobin, 2009, Vol.33 (6), p.422-427

2009

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Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysis

Prenatal diagnosis, 2007-07, Vol.27 (7), p.638-640

2007

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Novel 27.9 kb α 0 ‐thalassemia deletion in a Filipino woman

Digging deeper into the limits of ancient DNA research on syphilis

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

Novel 27.9 kb alpha(0)-thalassemia deletion in a Filipino woman

Molecular Characterization of a Novel 55.1 kb Gγ(Aγδβ)0-thalassemia Deletion in Two Canadian Families

Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC)

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 Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T)

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)

Characterisation of a novel 49.3 kb Ggamma(Agamma delta beta)(0) -thalassaemia deletion in seven families of Asian descent

Characterisation of a novel 49·3 kb Gγ(Aγδβ)0‐thalassaemia deletion in seven families of Asian descent

Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC)

Improved DNA extraction from ancient bones using silica-based spin columns

Evaluation of the CapillaryS 2 CE System for Hemoglobinopathy Investigations

Hb H hydrops foetalis syndrome: a case report and review of literature

Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutations

Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG)

Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families

Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysis

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