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Unusual combination of genetic defects in a Sicilian family: β-thalassaemia, haemoglobin Lepore Boston-Washington and heterocellular hereditary persistence of fetal haemoglobin

✍ Scribed by G. Schilirò; S. Musumeci; M. A. Romeo; F. Di Gregorio; A. Russo; R. Testa; G. Russo


Book ID
114710084
Publisher
John Wiley and Sons
Year
1983
Tongue
English
Weight
298 KB
Volume
55
Category
Article
ISSN
0007-1048

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