Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β(°)-thalassemia deletion

समान संसाधन

• DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2).
  द्वारा: Poncz, M, और अन्य
  प्रकाशित: (1987)
• Challenges in prenatal diagnosis and genetic counselling in compound heterozygosity for beta thalassemia and hereditary persistence of fetal hemoglobin (HPFH)
  द्वारा: Dolat Singh Shekhawat, और अन्य
  प्रकाशित: (2025-06-01)
• Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent β-thalassemia
  द्वारा: Huisman, T. H. J., और अन्य
  प्रकाशित: (1970)
• Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
  द्वारा: Zhang, Jie, और अन्य
  प्रकाशित: (2019)
• Hereditary persistence of fetal hemoglobin
  द्वारा: Sharma, Dharmesh Chandra, और अन्य
  प्रकाशित: (2020)