Screening and genetic diagnosis of haemoglobin disorders (Q35029576)

5 August 2017

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title

Screening and genetic diagnosis of haemoglobin disorders (English)

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5 August 2017

Old JM

1

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5 August 2017

language of work or name

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1 March 2003

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5 August 2017

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5 August 2017

volume

17

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5 August 2017

issue

1

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5 August 2017

page(s)

43-53

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Genetic diseases of hemoglobin: diagnostic methods for elucidating beta-thalassemia mutations.

5 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

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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https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

The laboratory diagnosis of haemoglobinopathies

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https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

1 reference

7 January 2021

Molecular basis for dominantly inherited inclusion body beta-thalassemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Guidelines for the fetal diagnosis of globin gene disorders. Globin Gene Disorder Working Party of the BCSH General Haematology Task Force

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

A β°-thalassaernia due to a 1605 bp deletion of the 5‘ β-globin gene region

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Prenatal diagnosis of beta-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Reverse dot-blot detection of Thai beta-thalassaemia mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Rapid detection and prenatal diagnosis of beta-thalassaemia: studies in Indian and Cypriot populations in the UK

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

The amplification refractory mutation system (ARMS): a rapid and direct prenatal diagnostic technique for beta-thalassaemia in Singapore

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Detection of specific DNA sequences by fluorescence amplification: a color complementation assay

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Rapid diagnosis of beta-thalassaemia by mutagenically separated polymerase chain reaction (MS-PCR) and its application to prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common β-thalassaemia mutations in Mediterraneans

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletions

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Filipino beta-thalassemia due to a large deletion: identification of the deletion endpoints and polymerase chain reaction (PCR)-based diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Detection of beta-thalassaemia mutations using DNA heteroduplex generator molecules

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Detection of common deletional alpha-thalassemia-2 determinants by PCR

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCA

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Direct detection of haemoglobin E with MnlI

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

A simplified procedure for sequencing amplified DNA containing the alpha 2- or alpha 1-globin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Characterization of the breakpoint of a 3.5-kb deletion of the beta-globin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2802%2900061-9

7 January 2021

10.1016/S0268-960X(02)00061-9

Identifiers

DOI

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5 August 2017

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