HUM-MOLGEN DIAGnostics/Clinical Research



SYNPOLYDACTYLY (Syndactyly TypeII): Our group is studying dominant synpolydactyly (OMIM 186000), which has been mapped to chromosome 2q31. We are keen to hear of further patients (with syndactyly of 3rd/4th fingers and 4th/5th toes, and extra digit in syndactylous web), who would be willing to provide blood samples to assist us in our project to find and analyse mutations in the synpolydactyly gene.

Please contact:

Dr. FR Goodman (Molecular Medicine Unit)
Prof RM Winter (Clinical Genetics Unit) Institute of Child Health, 30 Guilford St., London WC1N 1EH UK
tel 44 171 242 9789 Ext 2432 fax 44 171 831 0488