(Q34371372)

1 August 2017

title

Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases (English)

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1 August 2017

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6

Olivieri NF

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1 August 2017

Waye JS

1

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1 August 2017

Eng B

2

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1 August 2017

Patterson M

3

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1 August 2017

Walker L

4

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1 August 2017

Carcao MD

5

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1 August 2017

Chui DH

7

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1 August 2017

language of work or name

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1 September 2001

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American Journal of Hematology

1 August 2017

published in

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1 August 2017

volume

68

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1 August 2017

issue

1

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1 August 2017

page(s)

11-15

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1 August 2017

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The diverse molecular basis and mild clinical picture of HbH disease in Israel.

21 January 2018

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

21 January 2018

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Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

21 January 2018

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A PCR-based strategy to detect the common severe determinants of alpha thalassaemia

21 January 2018

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Locus assignment of human alpha globin mutations by selective amplification and direct sequencing

21 January 2018

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DNA sequencing with chain-terminating inhibitors

21 January 2018

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Practical guide to the diagnosis of thalassemia. Council of Regional Networks for Genetic Services (CORN).

21 January 2018

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Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?

21 January 2018

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Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients

21 January 2018

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HbH disease in Sardinia: molecular, hematological and clinical aspects

21 January 2018

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Molecular defects in Hb H hydrops fetalis

21 January 2018

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A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient

21 January 2018

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Phenotype-genotype correlation in haemoglobin H disease in childhood.

21 January 2018

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alpha-Thalassaemia in the population of Cyprus

21 January 2018

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Molecular pathology of haemoglobin H disease in Sardinians

21 January 2018

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Phenotype-genotype correlation in Sicilian patients with Hb H

21 January 2018

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Molecular basis and hematological characterization of Hb H disease in southeast Asia

21 January 2018

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Genetic and clinical features of hemoglobin H disease in Chinese patients

21 January 2018

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Different forms of Hb H disease in the Chinese

21 January 2018

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Characterization of two deletions that remove the entire human zeta-alpha globin gene complex (- -THAI and - -FIL)

21 January 2018

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PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletions

21 January 2018

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Novel mutation of the alpha 2-globin gene initiation codon (ATG-->A-G) in a Vietnamese girl with Hb H disease

21 January 2018

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The laboratory diagnosis of haemoglobinopathies

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/AJH.1142

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1 August 2017

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