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Coinheritance of two rare genodermatoses (Papillon–Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study

✍ Scribed by C. Hewitt; C-L. Wu; F.N. Hattab; W. Amin; K.A. Ghaffar; C. Toomes; P. Sloan; A.P. Read; J.A. James; N.S. Thakker


Book ID
108667806
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
231 KB
Volume
151
Category
Article
ISSN
0007-0963

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