✦ LIBER ✦
Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identifiedGLI3 mutations
✍ Scribed by Debeer, Philippe ;Peeters, H. ;Driess, S. ;De Smet, L. ;Freese, K. ;Matthijs, G. ;Bornholdt, D. ;Devriendt, K. ;Grzeschik, K.-H. ;Fryns, J.-P. ;Kalff-Suske, M.
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 310 KB
- Volume
- 120A
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.