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A frequentAγ-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia

✍ Scribed by S. Ottolenghi; C. Camaschella; P. Comi; B. Giglioni; M. Longinotti; L. Oggiano; F. Dore; G. Sciarratta; G. Ivaldi; G. Saglio; A. Serra; A. Loi; M. Pirastu

Publisher
Springer
Year
1988
Tongue
English
Weight
607 KB
Volume
79
Category
Article
ISSN
0340-6717

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📜 SIMILAR VOLUMES

Heterocellular hereditary persistence of
Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal γ-gene expression in association withβthalassemia and linkage relationship with theβ-globin gene cluster
✍ A. Giampaolo; F. Mavilio; N. M. Sposi; A. Carè; A. Massa; L. Cianetti; M. Petrin 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 663 KB

We report a study of four families of Italian origin in which heterocellular HPFH is inherited linked to beta thalassemia over two or three generations. The HPFH + beta thalassemia carriers showed thalassemic blood pictures and elevated HbF and F-cell number without increase in the HbF/F-cell conten