Literature DB >> 6345012

[Hereditary anemia: genetic basis, clinical characteristics, diagnosis and treatment. WHO Workgroup].

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Year:  1983        PMID: 6345012      PMCID: PMC2536125     

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN: 0042-9686            Impact factor:   9.408


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  8 in total

1.  Total management of thalassaemia major.

Authors:  B Modell
Journal:  Arch Dis Child       Date:  1977-06       Impact factor: 3.791

2.  Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin.

Authors:  D Tuan; M J Murnane; J L deRiel; B G Forget
Journal:  Nature       Date:  1980-05-29       Impact factor: 49.962

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

Authors:  Y W Kan; A M Dozy
Journal:  Lancet       Date:  1978-10-28       Impact factor: 79.321

4.  Structure and expression of a cloned beta o thalassaemic globin gene.

Authors:  N Moschonas; E de Boer; F G Grosveld; H H Dahl; S Wright; C K Shewmaker; R A Flavell
Journal:  Nucleic Acids Res       Date:  1981-09-11       Impact factor: 16.971

5.  An intron nucleotide sequence variant in a cloned beta +-thalassaemia globin gene.

Authors:  D Westaway; R Williamson
Journal:  Nucleic Acids Res       Date:  1981-04-24       Impact factor: 16.971

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

Authors:  M Busslinger; N Moschonas; R A Flavell
Journal:  Cell       Date:  1981-12       Impact factor: 41.582

7.  Major rearrangement in the human beta-globin gene cluster.

Authors:  R W Jones; J M Old; R J Trent; J B Clegg; D J Weatherall
Journal:  Nature       Date:  1981-05-07       Impact factor: 49.962

8.  Defective synthesis of HbE is due to reduced levels of beta E mRNA.

Authors:  J Traeger; W G Wood; J B Clegg; D J Weatherall
Journal:  Nature       Date:  1980-12-04       Impact factor: 49.962

  8 in total

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