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CEPH (Centre d'Etude du Polymorphisme Humain, Paris) 1991.
European Chromosome 21 Consortium (EC Human Genome Analysis and BIOMED Programmes) 1991-1998.
NIDCD Hereditary Hearing Impairment Consortium 1999.
OMIM (Online Mendelian Inheritance in Man, Database Catalog of Human Genes and Genetic Disorders), Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, 2001. |
