Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-021-01412-1.pdf
Reference5 articles.
1. Vyas P, Higgs DR, Weatherall DJ, Dunn D, Serjeant BE, Serjeant GR (1988) The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia. Br J Haematol 70(4):449–454
2. Serjeant GR, Serjeant BE, Fraser RA, Hambleton IR, Higgs DR Kulozik AE, Donaldson A (2011) Hb S-β-thalassemia: molecular, hematological and clinical comparisons. Hemoglobin 35(1):1–12
3. Garewal G, Das R, Ahluwalia J, Marwaha RK, Varma S (2005) Nucleotide− 88 (C-T) promoter mutation is a common β-thalassemia mutation in the Jat Sikhs of Punjab, India. Am J Hematol 79(4):252–256
4. Atweh GF, Forget BG (1987) Clinical and molecular correlations in the sickle/beta+-thalassemia syndrome. Am J Hematol 24(1):31–36
5. Mukherjee MB, Nadkarni AH, Gorakshakar AC, Ghosh K, Mohanty D, Colah RB (2010) Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India. Indian J Hum Genet 16(3):154–158
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