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Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and β-thalassaemia trait: partial correction of HS phenotype

✍ Scribed by Emanuele Miraglia del Giudice; Silverio Perrotta; Bruno Nobili; Luciano Pinto; Luisa Cutillo; Achille Iolascon


Book ID
114713285
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
602 KB
Volume
85
Category
Article
ISSN
0007-1048

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