domingo, 2 de diciembre de 2018

Primary immunodeficiency - OMIM - NCBI

Primary immunodeficiency - OMIM - NCBI

a toddler looking out a wiindow

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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IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED
Cytogenetic locations: 11q23.3
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