DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia

Схожие документы

• Interaction of Hb Adana (HBA2: c.179G>A) with Deletional and Nondeletional α (+)-Thalassemia Mutations: Diverse Hematological and Clinical Features
  по: Nainggolan, Ita M., et al.
  Опубликовано: (2013)
• Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent
  по: Tampaki, A, et al.
  Опубликовано: (2020)
• A novel gap-PCR with high resolution melting analysis for the detection of α-thalassaemia Southeast Asian and Filipino β(0)-thalassaemia deletion
  по: Leng Kho, Siew, et al.
  Опубликовано: (2015)
• Severe α-Thalassemia Intermedia Due to a Compound Heterozygosity for the Highly Unstable Hb Adana (HBA2: c.179G>A) and a Novel Codon 24 (HBA2: c.75T>A) Mutation
  по: Megawati, Dewi, et al.
  Опубликовано: (2014)
• Genetic and molecular diversity in nondeletion Hb H disease
  Опубликовано: (1982)