Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
about
Detection of Compound Heterozygous Sickle Cell-β+ Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia - A Case Report.Sickle cell disease: a neglected chronic disease of increasing global health importanceImpaired pre-mRNA processing and altered architecture of 3' untranslated regions contribute to the development of human disorders.Sickle cell/β-thalassemia: Comparison of Sβ0 and Sβ+ Brazilian patients followed at a single institution.The compound state: Hb S/beta-thalassemiaHb 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.Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children.Non-thalassemic phenotype associated with the -83 (G > A) mutation of the β-globin gene promoter (HBB: c.-133G > A).Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A).
P2860
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P2860
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
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2011年學術文章
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2011年學術文章
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name
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
@en
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
@nl
type
label
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
@en
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
@nl
prefLabel
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
@en
Hb S-β-thalassemia: molecular, hematological and clinical comparisons.
@nl
P2093
P2860
P1433
P1476
Hb S-β-thalassemia: molecular, hematological and clinical comparisons
@en
P2093
Alan Donaldson
Andreas E Kulozik
Beryl E Serjeant
Graham R Serjeant
Raphael A Fraser
P2860
P356
10.3109/03630269.2010.546306
P577
2011-01-01T00:00:00Z