The impact of Genetic Medicine on common and rare genetic disorders
|Submitted:||Friday 4th of November 2011 01:09:06 PM|
|Educational levels:||expert, qc2, qc3|
This resource is part of the following learning package:
Giovanni Romeo. The impact of Genetic Medicine on common and rare genetic disorders. EUROGENE portal. November 2011. online: http://eurogene.open.ac.uk/content/impact-genetic-medicine-common-and-rare-genetic-disorders-0
Keywordsaffected, affected sibpair, allele, Analysis of the entire coding region: Sequence analysis, association, association studies, autism, autosomal recessive, base, base pair, carrier, carrier screening, case-control, cell, centimorgan, chromosome, common disease, community genetics, complex disease, congenital, consanguineous, consanguineous marriage, consanguinity, de novo, deletion, deoxyribonucleic acid, duplication, dysplasia, environmental factor, enzyme, exon, expression, familial, family history, fixed, fluorescent in situ hybridization, founder, frequency, gene, gene locus, gene pool, genetic counselling, genetic counsellor, genetic disease, genetic predisposition, genetic variation, genetics, genome, genome wide association, genomics, genotype, haplotype, Healthcare Activity
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