A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India

Page 1

	Year	Citations
Inherited haemoglobin disorders: an increasing global health problem. D. J. Weatherall, J. B. Clegg PubMed Genetic EpidemiologyHigh FrequencyNon-communicable DiseaseAnemiaHematology	2001	1.2K
Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily Aurelio Maggio, Antonino Giambona, SP Cai, Blood	1993	169
Determination of the breakpoint and molecular diagnosis of a common α‐thalassaemia‐1 deletion in the Indian population Shaji R Velayudhan, S. E. Eunice, S. Baidya, British Journal of Haematology	2003	51
Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations. Antonino Giambona, Cristina Passarello, Gaetano Ruggeri, PubMed New MutationsGeneticsHuman PolymorphismPathologyDelta-globin Gene Mutations	2006	35
Hb lulu island (α<sub>2</sub>β<sub>2</sub>107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia G R Gray, Heather Manson, L‐H. Gu, American Journal of Hematology BiologyThalassemia IntermediaLaboratory HematologyGenetic DisorderMedicine	1995	15

Page 1