DiGeorge/Velocardiofacial Syndrome/congenital heart defect

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Topic: DiGeorge/Velocardiofacial Syndrome/congenital heart defect

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Administrator

posted 03-31-2000 03:35 PM

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.,
LONDON
WC1N 1EH UK
Tel 44 207 905 2635
Fax 44 207 831 0488 (or 404 6191)
email p.scambler@ich.ucl.ac.uk
pscamble@hgmp.mrc.ac.uk
http://www.ich.ucl.ac.uk/units/unitdes.html

IP: 160.45.191.21

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