Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks.
about
Results of topotecan single-agent therapy in patients with myelodysplastic syndromes and chronic myelomonocytic leukemia.Standards and guidelines for CFTR mutation testing.A melting curve analysis--based PCR assay for one-step genotyping of β-thalassemia mutations a multicenter validationComplete blood count reference intervals for healthy Han Chinese adults.Prenatal screening for cystic fibrosis: past, present and future.Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC).Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversity.Molecular basis of beta-thalassemia in the population of Tunisia.Compound heterozygosity for two new mutations in the beta-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA-->AAAAAA)] leads to thalassemia intermedia in a Tunisian patient.Molecular Diagnosis of Thalassemias and Hemoglobinopathies: An ACLPS Critical Review.Identification of Mediterranean beta-thalassemia mutations by reverse dot-blot in Italians and Egyptians.Advances in the prenatal and molecular diagnosis of the hemoglobinopathies and thalassemias.Molecular basis of asymptomatic beta-thalassemia major in an African American individual.Measurement of HbA1c and HbA2 by Capillarys 2 Flex Piercing HbA1c programme for simultaneous management of diabetes and screening for thalassemia.Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study.Three new beta-globin gene promoter mutations identified through newborn screening.Spectrum of hemoglobinopathies in Orissa, India.The beta+-IVS-I-6 (T-->C) mutation accounts for half of the thalassemia chromosomes in the Palestinian populations of the mountain regions.beta-Globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays.Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation.A new high A2-beta-thalassemia due to a 468 bp deletion (-475 to -8) in the beta-globin gene promoter of the intact beta-globin structural gene.The performance of MALBAC and MDA methods in the identification of concurrent mutations and aneuploidy screening to diagnose beta-thalassaemia disorders at the single- and multiple-cell levels.The phenomena of balanced effect between α-globin gene and of β-globin gene
P2860
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P2860
Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh
1994年學術文章
@zh-hant
name
Reverse dot blot probes for th ...... in Asians and American blacks.
@en
Reverse dot blot probes for th ...... in Asians and American blacks.
@nl
type
label
Reverse dot blot probes for th ...... in Asians and American blacks.
@en
Reverse dot blot probes for th ...... in Asians and American blacks.
@nl
prefLabel
Reverse dot blot probes for th ...... in Asians and American blacks.
@en
Reverse dot blot probes for th ...... in Asians and American blacks.
@nl
P2093
P356
P1433
P1476
Reverse dot blot probes for th ...... in Asians and American blacks.
@en
P2093
P356
10.1002/HUMU.1380030110
P577
1994-01-01T00:00:00Z