(Q39624723)

English

A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin

scientific article published on May 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

0 references

Hereditary persistence of fetal hemoglobin

0 references

author name string

Zertal-Zidani S

1

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Merghoub T

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Ducrocq R

3

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Gerard N

4

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Satta D

5

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Krishnamoorthy R

6

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

publication date

1 May 1999

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

23

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

159-169

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach.

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

A novel C-T transition within the distal CCAAT motif of the Gγ-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

Evaluation of high performance liquid chromatography for routine estimation of haemoglobins A2 and F

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expression.

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

A Taq 1 gamma-globin DNA polymorphism: an African-specific marker

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

Differential binding of the NFE3 and CP1/NFY transcription factors to the human gamma- and epsilon-globin CCAAT boxes.

1 reference

https://api.crossref.org/works/10.3109%2F03630269908996160

21 January 2018

Identifiers

10.3109/03630269908996160

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 September 2017

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