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Author Topic:   craniometaphyseal dysplasia
posted 07-07-2001 12:02 AM     Click Here to See the Profile for ereichen   Click Here to Email ereichen     Edit/Delete Message Reply w/Quote
Dear Colleagues,

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

Tel 617-456-7717
Fax 617-437-9822
email ereichenberger@forsyth.org


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