Literature DB >> 23729728

Unusual low sickle cell hemoglobin level.

Faouzi Baklouti, Jean Delaunay.   

Abstract

Keywords:  HBB cell; hemopoietic lineage; loss of heterozygosity; sickle cell

Mesh：

Substances：

Year:  2013        PMID： 23729728      PMCID： PMC3669458          DOI： 10.3324/haematol.2013.087973

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  3 in total

1.  HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype.

Authors:  Philippe Joly; Caroline Schluth-Bolard; Philippe Lacan; Claire Barro; Serge Pissard; Audrey Labalme; Damien Sanlaville; Catherine Badens
Journal:  Haematologica       Date:  2012-10-12       Impact factor: 9.941

2.  Beta+-thalassemia in cis of a sickle cell gene: occurrence of a promoter mutation on a beta s chromosome.

Authors:  F Baklouti; R Ouazana; C Gonnet; A Lapillonne; J Delaunay; J Godet
Journal:  Blood       Date:  1989-10       Impact factor: 22.113

3.  Association in cis of beta +-thalassemia and hemoglobin S.

Authors:  F Baklouti; A Francina; E Dorléac; G Richard; D Rosenberg; J Godet; J Delaunay
Journal:  Am J Hematol       Date:  1987-11       Impact factor: 10.047
  3 in total

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