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Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: Further delineation of the phenotype including 40 years follow-up

✍ Scribed by Mostert, A.K. ;Dijkstra, P.F. ;Jansen, B.R.H. ;van Horn, J.R. ;de Graaf, B. ;Heutink, P. ;Lindhout, D.


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
258 KB
Volume
120A
Category
Article
ISSN
0148-7299

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