Using Online Mendelian Inheritance in Man in low- and middle-income countries

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dc.contributor.authorMacena Sobreira, Nara Lygia de
dc.contributor.authorRepetto, Gabriela
dc.contributor.authorTemtamy, Samia A.
dc.contributor.authorAlvarez Perez, Ana Beatriz
dc.date.accessioned2021-12-28T16:07:41Z
dc.date.available2021-12-28T16:07:41Z
dc.date.issued2021
dc.description.abstractOnline Mendelian Inheritance in Man (OMIMĀ®), an online catalog of human genes and genetic disorders, has been used in the low- and middle-income countries largely as a tool for improving clinical care, teaching genetics and genomics, and for clinical and research analysis of next-generation sequencing. By facilitating free access to curated, updated, and comprehensive information in genetics and genomics, OMIM has led to better clinical care and research advancement in countries where clinicians and researchers in private or public hospitals and universities cannot afford to pay for other resources including journal subscriptions.es
dc.identifier.citationde Macena Sobreira NL, Repetto GM, Temtamy SA, Alvarez Perez AB. Using Online Mendelian Inheritance in Man in low- and middle-income countries. Am J Med Genet A. 2021 Nov;185(11):3284-3286. doi: 10.1002/ajmg.a.62467.es
dc.identifier.urihttps://doi.org/10.1002/ajmg.a.62467es
dc.identifier.urihttp://hdl.handle.net/11447/5298
dc.language.isoenes
dc.subjectDiagnosises
dc.subjectEducationes
dc.subjectLow-income countrieses
dc.subjectMiddle-income countrieses
dc.subjectOMIMes
dc.subjectRare diseaseses
dc.titleUsing Online Mendelian Inheritance in Man in low- and middle-income countrieses
dc.typeArticlees
dcterms.sourceAmerican Journal of Medical Genetics Part Aes

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