Statistika:
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Info omim.org:
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative
compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-t
(Rohkem)
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative
compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text,
referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes.
OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries
contain copious links to other genetics resources.
(Vähem)
Märksõnad:
Mendelian Inheritance in Man,
OMIM,
Mendelian diseases,
Mendelian disorders,
genetic diseases,
genetic disorders,
genetic disorders in humans,
genetic phenotypes,
phenotype and genotype,
disease models,
alleles,
genes,
dna,
genetics,
dna testing,
gene testing,
clinical synopsis,
medical genetics
(Vähem)
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