lunes, 2 de julio de 2018

Cardiomyopathy - OMIM - NCBI

Cardiomyopathy - OMIM - NCBI

Cardiomyopathy

From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.





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CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22, INCLUDED; CMH22, INCLUDED
Cytogenetic locations: 10q21.3
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