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  DiGeorge/Velocardiofacial Syndrome/congenital heart defect

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Author Topic:   DiGeorge/Velocardiofacial Syndrome/congenital heart defect
posted 03-31-2000 03:35 PM     Click Here to See the Profile for Administrator     Edit/Delete Message Reply w/Quote
Call for Patients:

DiGeorge/VCFS without Chromosome 22q11 Deletion

We are interested in DNA samples from patients with a clinical diagnosis of probable DiGeorge/velocardiofacial syndrome but no deletion at 22q11 for our on going point mutation screening programme. Patients with congenital heart defects seen in DGS/VCFS will also be welcomed. It would be helpful, but not essential, if parental samples were also available.

Contact person:

Prof. Peter Scambler,
Room 211,
Molecular Medicine Unit,
Institute of Child Health,
30 Guilford St.,
Tel 44 207 905 2635
Fax 44 207 831 0488 (or 404 6191)
email p.scambler@ich.ucl.ac.uk


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