(Q57953390)

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Hereditary anaemias: genetic basis, clinical features, diagnosis, and treatment. WHO working group

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title

Hereditary anaemias: genetic basis, clinical features, diagnosis, and treatment. WHO working group (English)

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main subject

diagnosis

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language of work or name

English

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publication date

1982

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published in

Bulletin of the World Health Organization

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volume

60

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page(s)

643-60

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issue

5

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cites work

Beta + thalassemia: aberrant splicing results from a single point mutation in an intron.

1 reference

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PubMed Central

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Structure and expression of a cloned beta o thalassaemic globin gene

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30 November 2018

An intron nucleotide sequence variant in a cloned β+-thalassaemia globin gene

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536044

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30 November 2018

Total management of thalassaemia major

1 reference

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PubMed Central

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30 November 2018

Antenatal diagnosis of sickle-cell anaemia by D.N.A. analysis of amniotic-fluid cells

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30 November 2018

Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin

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reference URL

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retrieved

12 December 2020

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Defective synthesis of HbE is due to reduced levels of βE mRNA

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6983923

retrieved

12 December 2020

based on heuristic

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Major rearrangement in the human β-globin gene cluster

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6983923

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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(Q57953390)

Hereditary anaemias: genetic basis, clinical features, diagnosis, and treatment. WHO working group

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