Literature DB >> 7073867

Sickle cell-hemoglobin D Iran: benign sickle cell syndrome.

B Serjeant, E Myerscough, G R Serjeant, D R Higgs, W F Moo-Penn.   

Abstract

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Year:  1982        PMID： 7073867     DOI： 10.3109/03630268208996934

Source DB:  PubMed          Journal:  Hemoglobin        ISSN： 0363-0269            Impact factor:   0.849


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  5 in total

1.  Compound heterozygous hemoglobin d-punjab/hemoglobin d-iran: a novel hemoglobinopathy.

Authors:  Aastha Gupta; Amrita Saraf; Jasmita Dass; Meenal Mehta; Nita Radhakrishnan; Renu Saxena; Manorama Bhargava
Journal:  Indian J Hematol Blood Transfus       Date:  2014-08-08       Impact factor: 0.900

2.  Hb D: A Not So Rare Hemoglobinopathy.

Authors:  A M Shanthala Devi; Karuna Rameshkumar; S Sitalakshmi
Journal:  Indian J Hematol Blood Transfus       Date:  2014-01-22       Impact factor: 0.900

3.  Comparison of the characteristics of two hemoglobin variants, Hb D-Iran and Hb E, eluting in the Hb A2 window.

Authors:  Jasmita Dass; Aastha Gupta; Suchi Mittal; Amrita Saraf; Sabina Langer; Manorama Bhargava
Journal:  Blood Res       Date:  2017-06-22

4.  Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India.

Authors:  Pradeep Kumar Mohanty; Satyabrata Meher; Snehadhini Dehury; Subhra Bhattacharya; Kishalaya Das; Siris Patel; Biswanath Sarkar
Journal:  Rev Bras Hematol Hemoter       Date:  2017-12-01

5.  Comments on: "Clinical, hematological and genetic data of a cohort of children with hemoglobin SD".

Authors:  Maria Stella Figueiredo
Journal:  Rev Bras Hematol Hemoter       Date:  2016-06-22
  5 in total

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