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Screening and genetic diagnosis of haemoglobin disorders
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Screening and genetic diagnosis of haemoglobin disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
author name string
Old JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
language of work or name
English
1 reference
based on heuristic
inferred from title
publication date
1 March 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
published in
Blood Reviews
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
volume
17
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
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5 August 2017
page(s)
43-53
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Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
cites work
Genetic diseases of hemoglobin: diagnostic methods for elucidating beta-thalassemia mutations.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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Guidelines for investigation of the alpha and beta thalassaemia traits. The Thalassaemia Working Party of the BCSH General Haematology Task Force
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Crossref
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https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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The laboratory diagnosis of haemoglobinopathies
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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Beta-thalassaemia
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https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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Molecular basis for dominantly inherited inclusion body beta-thalassemia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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inferred from DOI database lookup
Guidelines for the fetal diagnosis of globin gene disorders. Globin Gene Disorder Working Party of the BCSH General Haematology Task Force
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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A β°-thalassaernia due to a 1605 bp deletion of the 5‘ β-globin gene region
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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Prenatal diagnosis of beta-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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based on heuristic
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Reverse dot-blot detection of Thai beta-thalassaemia mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Rapid detection and prenatal diagnosis of beta-thalassaemia: studies in Indian and Cypriot populations in the UK
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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The amplification refractory mutation system (ARMS): a rapid and direct prenatal diagnostic technique for beta-thalassaemia in Singapore
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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Detection of specific DNA sequences by fluorescence amplification: a color complementation assay
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Rapid diagnosis of beta-thalassaemia by mutagenically separated polymerase chain reaction (MS-PCR) and its application to prenatal diagnosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common β-thalassaemia mutations in Mediterraneans
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletions
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Filipino beta-thalassemia due to a large deletion: identification of the deletion endpoints and polymerase chain reaction (PCR)-based diagnosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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inferred from DOI database lookup
Detection of beta-thalassaemia mutations using DNA heteroduplex generator molecules
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
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Detection of common deletional alpha-thalassemia-2 determinants by PCR
1 reference
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Crossref
reference URL
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7 January 2021
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A PCR-based strategy to detect the common severe determinants of alpha thalassaemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis of Hb H disease due to compound heterozygosity for South-east Asian deletion and Hb constant spring by polymerase chain reaction
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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inferred from DOI database lookup
Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCA
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Direct detection of haemoglobin E with MnlI
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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A simplified procedure for sequencing amplified DNA containing the alpha 2- or alpha 1-globin gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Characterization of the breakpoint of a 3.5-kb deletion of the beta-globin gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9
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7 January 2021
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Identifiers
DOI
10.1016/S0268-960X(02)00061-9
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
PubMed ID
12490210
1 reference
stated in
Europe PubMed Central
PubMed ID
12490210
retrieved
5 August 2017
ResearchGate publication ID
10984249
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