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. 2002 Feb;39(2):110–112. doi: 10.1136/jmg.39.2.110
Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13
M Abramowicz
1, J Albuquerque-Silva
1, A Zanen
1
M Abramowicz
1Laboratoire de Génétique Médicale, Hôpital Erasme-ULB, 808 Route de Lennik, B-1070 Brussels, Belgium. marcabra@ulb.ac.be
Find articles by M Abramowicz
J Albuquerque-Silva
1Laboratoire de Génétique Médicale, Hôpital Erasme-ULB, 808 Route de Lennik, B-1070 Brussels, Belgium. marcabra@ulb.ac.be
Find articles by J Albuquerque-Silva
A Zanen
1Laboratoire de Génétique Médicale, Hôpital Erasme-ULB, 808 Route de Lennik, B-1070 Brussels, Belgium. marcabra@ulb.ac.be
Find articles by A Zanen
1Laboratoire de Génétique Médicale, Hôpital Erasme-ULB, 808 Route de Lennik, B-1070 Brussels, Belgium. marcabra@ulb.ac.be
PMCID: PMC1735049 PMID: 11836359