Resultado de búsqueda
Mendelian Inheritance in Man es una base de datos de genes humanos y trastornos y rasgos genéticos, con un enfoque particular en la relación gen-fenotipo. Está disponible de forma telemática en la web de la Facultad de Medicina de la Universidad Johns Hopkins, [1] en la que se actualiza prácticamente a diario.
Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. As of 28 June 2019 [update] , approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes ; the rest represented genes , many of ...
- Catalog of all known human genes and genetic phenotypes.
- Johns Hopkins University School of Medicine
Hace 4 días · 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.
Mendelian inheritance (also known as Mendelism) is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866, re-discovered in 1900 by Hugo de Vries and Carl Correns, and later popularized by William Bateson.
Rasgos mendelianos en humanos. En la herencia mendeliana, un hijo que reciba el alelo dominante de uno de los padres, tendrá la forma dominante del rasgo o carácter. Sólo aquellos que hayan recibido el alelo recesivo de ambos padres, presentará el fenotipo recesivo.
Mendelian traits in humans are human traits that are substantially influenced by Mendelian inheritance. Most – if not all – Mendelian traits are also influenced by other genes, the environment, immune responses, and chance.
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.
