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

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

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

Research output: Contribution to journalArticleAcademicpeer-review

Translated title of the contributionFamilial multiple epiphyseal dysplasia due to a matrilin-3 mutation. Further delineation of the phenotype including 40 years follow-up
Original languageUndefined/Unknown
Pages (from-to)490-497
Number of pages8
JournalAmerican Journal of Medical Genetics. Part A
Volume120A
Issue number4
Publication statusPublished - 2003

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