𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster

✍ Scribed by G. Martinez; A. Novelletto; A. Rienzo; L. Felicetti; B. Colombo

Publisher
Springer
Year
1989
Tongue
English
Weight
257 KB
Volume
82
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Hemoglobin F production in heterocellula
Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the β globin gene complex
✍ J. A. Donald; A. Lammi; R. J. Trent 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 689 KB

Some types of nondeletional heterocellular hereditary persistence of fetal hemoglobin (HPFH) appear to be caused by mutations in the beta globin gene cluster near the gamma globin genes, while in other cases the condition is associated with a gene or genes outside the beta globin gene complex. We ha

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