Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)(0)-thalassemia in eastern India

Ítems similars

• Prevalence of Deletional Alpha Thalassemia and Sickle Gene in a Tribal Dominated Malaria Endemic Area of Eastern India
  per: Purohit, Prasanta, et al.
  Publicat: (2014)
• Inheritance of Hereditary Persistence of Fetal Haemoglobin (HPFH) in a Family of Western Odisha, India
  per: Patel, Siris, et al.
  Publicat: (2015)
• A Compound Heterozygous Asian Indian Inversion Deletion Gγ(Aγδβ)(0) with β-Thalassemia in Central India: A Case Report
  per: Lad, Harsha, et al.
  Publicat: (2017)
• Compound heterozygote of Hb D(Iran) [HBB: c.67G>C, β 22(B4) Glu>Gln] with β(0)-thalassemia [cds 41/42 (-CTTT)] from Eastern India
  per: Mohanty, Pradeep Kumar, et al.
  Publicat: (2018)
• Phenotypic Heterogeneity of Asian Indian Inversion Deletions Gγ(Aγδβ)0 Breakpoint A and Breakpoint B
  per: Pandey, Sanjay, et al.
  Publicat: (2012)