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  1. Hace 2 días · OMIM is a free and authoritative database of human genes and genetic disorders, updated daily. It provides referenced overviews of mendelian disorders and over 15,000 genes, with links to other genetics resources.

  2. Hace 2 días · OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, under the direction of Dr. Ada Hamosh.

  3. 1 de jul. de 2014 · Learn how to use the OMIM search engine to find information on human genes and genetic disorders. Find out how to use basic, advanced, and complex search options, such as operators, wildcards, fields, and dates.

  4. OMIM was developed as a catalog of Mendelian traits and disorders, with a focus on the relationship between phenotype and genotype. Description. OMIM is a comprehensive guide to human genes and genetic phenotypes with full-text, referenced overviews for all mendelian disorders and over 16,000 genes. Audience.

  5. Actualmente la versión en línea se denomina Online Mendelian Inheritance in Man (OMIM). El proyecto fue iniciado y desarrollado en los años 60 por el doctor Victor A. McKusick y colegas de la universidad Johns Hopkins.

  6. 1 de ene. de 2005 · Online Mendelian Inheritance in Man (OMIM™) is a comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics. Started by Dr Victor A. McKusick as the definitive reference Mendelian Inheritance in Man, OMIM ...

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