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

AK Mostert, PF Dijkstra, BRH Jansen, JR van Horn, Bianca de Graaf, P Heutink, D (Dick) Lindhout

Research output: Contribution to journalArticleAcademicpeer-review

37 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)490-497
Number of pages8
JournalAmerican Journal of Medical Genetics
Volume120
Publication statusPublished - 2003

Research programs

  • EMC MGC-02-96-01

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