posted 07-07-2001 12:02 AM            

We have recently identified a gene and mutations responsible for autosomal dominant craniometaphyseal dysplasia (CMD) and are now interested in additional CMD cases (isolated and familial) to identify new mutations and seek biopsy material for further studies. We are looking for collaborations with clinicians who have access to CMD patients.

Ernst Reichenberger
Harvard-Forsyth Department of Oral Biology
HSDM / Forsyth Institute
140 The Fenway
Boston MA 02115