𝔖 Bobbio Scriptorium
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APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas

✍ Scribed by B Filipe; C Baltazar; C Albuquerque; S Fragoso; P Lage; I Vitoriano; S Mão de Ferro; I Claro; P Rodrigues; P Fidalgo; P Chaves; M Cravo; C Nobre Leitão


Book ID
110888854
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
508 KB
Volume
76
Category
Article
ISSN
0009-9163

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