A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
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Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.Investigating alpha-globin structural variants: a retrospective review of 135,000 Brazilian individualsThe Hematological and Molecular Spectrum of α-Thalassemias in Turkey: The Hacettepe Experience.Prevalence of α-thalassaemia genotypes in pregnant women in northern ThailandMolecular diagnostics for haemoglobinopathies.Rapid confirmation of Southeast Asian and Filipino alpha-thalassemia genotypes from newborn screening specimens.Molecular basis of alpha-thalassemia in Algeria.First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion.A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West Iran.Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.Advances in the prenatal and molecular diagnosis of the hemoglobinopathies and thalassemias.Human alpha-thalassemia syndromes: detection of molecular defects.Haemoglobinopathies.Development of an ELISA strip for the detection of alpha thalassemias.Hb Bart's levels in cord blood and alpha-thalassemia mutations in Cyprus.A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene.Genetic and hematological studies in a group of 114 adult patients with SC sickle cell disease.alpha-globin genes: thalassemic and structural alterations in a Brazilian population.Rapid detection of the common Mediterranean alpha-globin deletions/rearrangements using PCR.A newly identified deletion of 970 bp at the alpha-globin locus that removes the promoter region of the alpha1 gene.Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features.α-Thalassemia syndromes in the United Arab Emirates.A family with multiple mutations and sequence variations in the alpha- and beta-globin gene clusters.Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],a new hemoglobin variant of the α2-globin gene.Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions.Molecular Characterization of Hereditary Persistence of Fetal Hemoglobin in the Karen People of Thailand
P2860
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P2860
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
1992年學術文章
@zh-hant
name
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@en
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@nl
type
label
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@en
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@nl
prefLabel
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@en
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@nl
P2093
P2860
P1476
A PCR-based strategy to detect the common severe determinants of alpha thalassaemia.
@en
P2093
P2860
P304
P356
10.1111/J.1365-2141.1992.TB08180.X
P407
P577
1992-05-01T00:00:00Z