State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies.

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Preconception carrier screening and prenatal diagnosis in thalassemia and hemoglobinopathies: challenges and future perspectives.Laboratory diagnosis of thalassemia.Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia.

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P2860

State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies.

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State of the art and new devel ...... hies in multiethnic societies.

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State of the art and new devel ...... hies in multiethnic societies.

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C L Harteveld

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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

A new alpha(0)-thalassemia deletion found in a Dutch family (--(AW)).

Screening and genetic diagnosis of haemoglobin disorders.

Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification.

Epidemiology of haemoglobin disorders in Europe: an overview.

An overview of current microarray-based human globin gene mutation detection methods.

Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing

Global epidemiology of haemoglobin disorders and derived service indicators.

Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.

Targeted therapeutic strategies for fetal hemoglobin induction.

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10.1111/IJLH.12108

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2013-05-31T00:00:00Z

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236975788

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State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies.

about

P2860

P2860

State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies.

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