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Clinical, molecular and biochemical characterization of nine Spanish families with Conradi–Hünermann–Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature

✍ Scribed by J. Cañueto; M. Girós; S. Ciria; G. Pi-Castán; M. Artigas; J. García-Dorado; V. García-Patos; A. Virós; T. Vendrell; A. Torrelo; Á. Hernández-Martín; E. Martín-Hernández; M.T. Garcia-Silva; M. Fernández-Burriel; J. Rosell; M. Tejedor; F. Martínez; J. Valero; J.L. García; E.M. Sánchez-Tapia; P. Unamuno; R. González-Sarmiento


Book ID
108672126
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
678 KB
Volume
166
Category
Article
ISSN
0007-0963

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