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16p proximal deletions - Unique - The Rare Chromosome Disorder ...

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<strong>Rare</strong> <strong>Chromosome</strong> <strong>Disorder</strong> Support Group Charity Number 1110661<br />

Registered in England and Wales Company Number 5460413<br />

16<br />

Support and Information<br />

<strong>Rare</strong> <strong>Chromosome</strong> <strong>Disorder</strong><br />

Support Group,<br />

PO Box 2189,<br />

Caterham,<br />

Surrey CR3 5GN,<br />

UK<br />

Tel/Fax: +44(0)1883 330766<br />

info@rarechromo.org<br />

www.rarechromo.org<br />

Photographs on front (bottom left) and on pages 11 & 13 by kind courtesy of Brian Cassey<br />

www.briancasseyphotographer.com<br />

This leaflet is not a substitute for personal medical advice. Families should consult a<br />

medically qualified clinician in all matters relating to genetic diagnosis, management<br />

and health. <strong>The</strong> information is believed to be the best available at the time of<br />

publication. It was compiled by <strong>Unique</strong> and reviewed by Dr Philip Giampetro,<br />

Department of Medical Genetics, Dr Shereif Rezkalla, Department of Cardiology,<br />

Marshfield Clinic, Marshfield, Wisconsin, USA and by Professor Maj Hulten BSc<br />

PhD MD FRCPath, Professor of Medical Genetics, University of Warwick, UK<br />

2007. Revised 06/2009: the new section on <strong>16p</strong>11.2 micro<strong>deletions</strong> was reviewed<br />

by Dr Emilia Bijlsma, clinical geneticist, Leiden University Medical Centre, <strong>The</strong><br />

Netherlands.<br />

Copyright © <strong>Unique</strong> 2009

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