Literature DB >> 22581004

A novel deletion of β-globin promoter causing high HbA2 in an Indian population.

Thiyagaraj Mayuranathan1, Janakiram Rayabaram, Eunice Sindhuvi Edison, Alok Srivastava, Shaji R Velayudhan.   

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Year:  2012        PMID： 22581004      PMCID： PMC3436249          DOI： 10.3324/haematol.2012.062299

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


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  5 in total

Review 1.  Databases of human hemoglobin variants and other resources at the globin gene server.

Authors:  R C Hardison; D H Chui; C Riemer; B Giardine; H Lehväslaiho; H Wajcman; W Miller
Journal:  Hemoglobin       Date:  2001-05       Impact factor: 0.849

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

Authors:  J E Craig; S J Kelly; R Barnetson; S L Thein
Journal:  Br J Haematol       Date:  1992-12       Impact factor: 6.998

3.  Molecular characterization of an atypical beta-thalassemia caused by a large deletion in the 5' beta-globin gene region.

Authors:  B W Popovich; D S Rosenblatt; A G Kendall; Y Nishioka
Journal:  Am J Hum Genet       Date:  1986-12       Impact factor: 11.025

4.  Gamma thalassemia resulting from the deletion of a gamma-globin gene.

Authors:  P K Sukumaran; T Nakatsuji; M B Gardiner; A L Reese; J G Gilman; T H Huisman
Journal:  Nucleic Acids Res       Date:  1983-07-11       Impact factor: 16.971

5.  Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification.

Authors:  C L Harteveld; A Voskamp; M Phylipsen; N Akkermans; J T den Dunnen; S J White; P C Giordano
Journal:  J Med Genet       Date:  2005-05-13       Impact factor: 6.318
  5 in total

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