HUM-MOLGEN DIAGnostics/Clinical Research


September, 1 1999
Fraser Syndrome (OMIM 219000) 
and 
Jeune syndrome (OMIM 208500)

We are searching for additional patients/families suitable for the homzygosity mapping of Fraser cryptopthalmos/syndactyly) Syndrome - (OMIM 219000) and Jeune (asphyxiating thoracic dystropy) syndrome (OMIM 208500).

If it is possible you would be able to obtain blood/DNA for such a study please contact Dr. Lesley McGregor (l.mcgregor@ich.ucl.ac.uk) or Prof Peter Scambler (postal address below).

Many thanks


Prof. Peter Scambler,
Room 211,
Molecular Medicine Unit,
Institute of Child Health,
30 Guilford St.,
LONDON
WC1N 1EH UK
Tel 44 207 905 2635 (or 242 9789 x2635)
Fax 44 207 831 0488 (or 404 6191)
alternative email p.scambler@ich.ucl.ac.uk
                            pscamble@hgmp.mrc.ac.uk
http://www.ich.ucl.ac.uk/  (see Academic Units - Molecular Medicine)