The impact of Genetic Medicine on common and rare genetic disorders
|Submitted:||Thursday 3rd of November 2011 09:14:35 AM|
|Content type:||Learning resource|
|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
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, haplotype block, hapmap project, hereditary, heredity, heterogeneous, heterozygous, hotspot, human genome project, human leucocyte antigen, hybrid, inherited, karyotype, kilobase, linkage, linkage analysis, linkage disequilibrium, locus, malformation, marker, mendelian disorder, minor allele frequency, monogenic, mutation, nucleotide, pedigree, penetrance, phase, phenotype, polymerase chain reaction, polymorphic marker, polymorphism, population, positional cloning, power, predisposing mutation, prevalence, probability, protein, recombination, relative risk, replication, ribonucleic acid, screening, selection, sequence, sib, single nucleotide polymorphism, splice site, syndrome, tagging snp, threshold, trait, variant, variation, x-chromosome
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. Read more.