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Next‐generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters

International journal of laboratory hematology, 2017-05, Vol.39 (S1), p.111-120

2017

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Genetic influences on F cells and other hematologic variables : a twin heritability study

Blood, 2000, Vol.95 (1), p.342-346

2000

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Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Human molecular genetics, 2009-10, Vol.18 (R2), p.R216-R223

2009

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Pulmonary function abnormalities in children with sickle cell disease

Thorax, 2004-01, Vol.59 (1), p.67-70

2004

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Molecular diagnosis of haemoglobin disorders

Clinical and laboratory haematology, 2004-06, Vol.26 (3), p.159-176

2004

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IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β‐CHAIN VARIANT THAT IS HIGHLY UNSTABLE?

British journal of haematology, 1999-10, Vol.107 (1), p.12-21

Thein, Swee Lay

1999

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Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis

Thrombosis and haemostasis, 1997-01, Vol.77 (1), p.197-211

1997

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Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?

British journal of haematology, 1998-01, Vol.100 (1), p.70-78

1998

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Haplotype Mapping of a Major Quantitative-Trait Locus for Fetal Hemoglobin Production, on Chromosome 6q23

American journal of human genetics, 1998-06, Vol.62 (6), p.1468-1474

1998

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Computed tomography and pulmonary function abnormalities in sickle cell disease

The European respiratory journal, 2006-10, Vol.28 (4), p.832-838

2006

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Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK

Annals of hematology, 2016-01, Vol.95 (2), p.227-232

2016

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Fetal hemoglobin levels in adults

Blood reviews, 1994-12, Vol.8 (4), p.213-224

1994

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The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes

Journal of community genetics, 2022-04, Vol.13 (2), p.229-234

2022

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Individual-specific 'fingerprints' of human DNA

Nature (London), 1985-01, Vol.316 (6023), p.76-79

1985

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Peak expiratory flow in Afro-Caribbean children with and without sickle cell anaemia

Acta Paediatrica, 2007-09, Vol.96 (9), p.1308-1310

2007

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Treatment of thalassaemia major with phenylbutyrate and hydroxyurea

The Lancet (British edition), 1997-08, Vol.350 (9076), p.491-492

1997

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Gene regulation and deregulation: a β globin perspective

Blood reviews, 2000-06, Vol.14 (2), p.78-93

2000

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Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African population

SAMJ: South African Medical Journal, 2016-03, Vol.106 (3), p.276-279

2016

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A simple and rapid method of direct sequencing using Dynabeads

British journal of haematology, 1991-09, Vol.79 (1), p.113-115

1991

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PS-208 Genetic Predisposition To The Development Of Bronchopulmonary Dysplasia In Infants Born Prematurely

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A187-A188

2014

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Molecular Basis for Dominantly Inherited Inclusion Body β-Thalassemia

Proceedings of the National Academy of Sciences - PNAS, 1990-05, Vol.87 (10), p.3924-3928

1990

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Determinants of iron status and bilirubin levels in congenital dyserythropoietic anaemia type I

British journal of haematology, 1999-12, Vol.107 (3), p.522-525

1999

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Genetic influences on F cells and other hematologic variables: a twin heritability study

Blood, 2000-01, Vol.95 (1), p.342-346

2000

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Interaction Between Two Quantitative Trait Loci Affects Fetal Haemoglobin Expression

Annals of human genetics, 2005-11, Vol.69 (6), p.707-714

2005

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Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers

American journal of human genetics, 1994-02, Vol.54 (2), p.214-228

1994

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Next‐generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters

Genetic influences on F cells and other hematologic variables : a twin heritability study

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Pulmonary function abnormalities in children with sickle cell disease

Molecular diagnosis of haemoglobin disorders

IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β‐CHAIN VARIANT THAT IS HIGHLY UNSTABLE?

Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis

Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?

Haplotype Mapping of a Major Quantitative-Trait Locus for Fetal Hemoglobin Production, on Chromosome 6q23

Computed tomography and pulmonary function abnormalities in sickle cell disease

Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK

Fetal hemoglobin levels in adults

The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes

Individual-specific 'fingerprints' of human DNA

Peak expiratory flow in Afro-Caribbean children with and without sickle cell anaemia

Treatment of thalassaemia major with phenylbutyrate and hydroxyurea

Gene regulation and deregulation: a β globin perspective

Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African population

A simple and rapid method of direct sequencing using Dynabeads

PS-208 Genetic Predisposition To The Development Of Bronchopulmonary Dysplasia In Infants Born Prematurely

Molecular Basis for Dominantly Inherited Inclusion Body β-Thalassemia

Determinants of iron status and bilirubin levels in congenital dyserythropoietic anaemia type I

Genetic influences on F cells and other hematologic variables: a twin heritability study

Interaction Between Two Quantitative Trait Loci Affects Fetal Haemoglobin Expression

Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers

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