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Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

โœ Scribed by Hamosh, A.


Book ID
126842568
Publisher
Oxford University Press
Year
2004
Tongue
English
Weight
260 KB
Volume
33
Category
Article
ISSN
0305-1048

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OMIM's task of cataloging the association between human phenotypes and their causative genes (the Morbid Map of the Genome) and classifying and naming newly recognized disorders is growing rapidly. Establishing the relationship between genotype and phenotype has become increasingly complex. New tech