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OMIN
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OMIM is a database of human genes and genetic disorders, updated daily and accessible to the public. It provides information on mendelian inheritance, phenotype-genotype relationships, and links to other genetics resources.
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.
OMIM is a free online resource that provides information on mendelian disorders and genes. It is updated daily and authored by experts at Johns Hopkins University.
OMIM is a database of human genes and genetic disorders that can be searched online or downloaded. To access the data files, users need to register and agree to the licensing terms and conditions.
OMIM is a free catalog of human genes and genetic disorders and traits, based on the peer-reviewed biomedical literature. It covers all known mendelian disorders and over 15,000 genes, and is updated continuously by the McKusick-Nathans Institute of Genetic Medicine.
OMIM is a database of human genes and genetic phenotypes, with a focus on the gene-phenotype relationship. It is maintained by Johns Hopkins University and used by researchers, health care professionals and students in genetics and medicine.
Online Mendelian Inheritance In Man (OMIM) is a public database of bibliographic information about human genes and genetic disorders. Begun by Dr. Victor McKusick as the authoritative reference Mendelian Inheritance in Man, it is now distributed electronically by the National Center for Biotechnolog …
OMIM is a comprehensive, online database of human inherited disorders and their genetic basis, developed by Johns Hopkins University. It provides detailed information, links to other resources, and a numbering system for each entry.
Web site: http://www.ncbi.nlm.nih.gov/omim/ Authority Online Mendelian Inheritance in Man ® (OMIM ®) was developed and is maintained by the McKusick-Nathans ...
(A) Entry for cystic fibrosis, which contains links to the CFMDB and the list of CF cell lines available for research. (B) An example of links from the CFTR entry to Nomenclature, RefSeq, GenBank, Protein and UniGene databases.An OMIM entry includes the primary title and symbol, alternative titles and symbols, and 'included' titles (i.e. related but not synonymous information that is not ...