lunes, 25 de diciembre de 2017

Personal stories - OMIM - NCBI

Personal stories - OMIM - NCBI

Personal Stories

From NIH OMIM

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



CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED
Cytogenetic locations: 3p22.2

No hay comentarios:

Publicar un comentario