Literature DB >> 34744353

Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis.

Diksha Dev Yadav1, Namrata Singh1, Sreejesh Sreedharanunni1, Jasbir Kaur Hira1, Sanjeev Chhabra1, Amita Trehan2, Subhash Saha3, Prashant Sharma1, Reena Das1.   

Abstract

Entities:  

Year:  2021        PMID： 34744353      PMCID： PMC8523634          DOI： 10.1007/s12288-021-01412-1

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN： 0971-4502            Impact factor:   0.915


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  5 in total

1.  Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India.

Authors:  Gurjeewan Garewal; Reena Das; Jasmina Ahluwalia; R K Marwaha; S Varma
Journal:  Am J Hematol       Date:  2005-08       Impact factor: 10.047

2.  Hb S-β-thalassemia: molecular, hematological and clinical comparisons.

Authors:  Graham R Serjeant; Beryl E Serjeant; Raphael A Fraser; Ian R Hambleton; Douglas R Higgs; Andreas E Kulozik; Alan Donaldson
Journal:  Hemoglobin       Date:  2011       Impact factor: 0.849

3.  Clinical and molecular correlations in the sickle/beta+-thalassemia syndrome.

Authors:  G F Atweh; B G Forget
Journal:  Am J Hematol       Date:  1987-01       Impact factor: 10.047

4.  The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.

Authors:  P Vyas; D R Higgs; D J Weatherall; D Dunn; B E Serjeant; G R Serjeant
Journal:  Br J Haematol       Date:  1988-12       Impact factor: 6.998

5.  Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India.

Authors:  Malay B Mukherjee; Anita H Nadkarni; Ajit C Gorakshakar; Kanjaksha Ghosh; Dipika Mohanty; Roshan B Colah
Journal:  Indian J Hum Genet       Date:  2010-09
  5 in total

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