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

Autor: de Macena Sobreira NL; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Repetto GM; Rare Diseases Program, Institute of Science and Innovation in Medicine, Facultad de Medicina Clinica Alemana Universidad del Desarrollo, Santiago, Chile., Temtamy SA; Department of Clinical Genetics, Division of Human Genetics and Genome Research, National Research Center, Cairo, Egypt., Alvarez Perez AB; Department of Morphology and Genetic, Federal University of São Paulo, São Paulo, Brazil.
Jazyk: angličtina
Zdroj: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Nov; Vol. 185 (11), pp. 3284-3286. Date of Electronic Publication: 2021 Sep 07.
DOI: 10.1002/ajmg.a.62467
Abstrakt: Online Mendelian Inheritance in Man (OMIM®), 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.
(© 2021 Wiley Periodicals LLC.)
Databáze: MEDLINE
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