A family with S and C hemoglobins and the hereditary persistence of F hemoglobin. A comparison of C thalassemia disease with the CF syndrome.

Subjects

Subjects :

Humans
Anemia, Sickle Cell genetics
Fetal Hemoglobin
Hemoglobins abnormalities
Thalassemia
beta-Thalassemia genetics

Details

Language :

English

ISSN :

0028-4793

Volume :

265

Database :

MEDLINE

Journal :

The New England journal of medicine

Publication Type :

Academic Journal

Accession number :

13908956

Full Text :

https://doi.org/10.1056/NEJM196112282652602