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Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): Report of a four-generation pedigree, identification of a mutation in TGFB1, and review

✍ Scribed by Wallace, Stephanie E. ;Lachman, Ralph S. ;Mekikian, Pertchoui B. ;Bui, Kathy K. ;Wilcox, William R.


Book ID
101454248
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
267 KB
Volume
129A
Category
Article
ISSN
0148-7299

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