viernes, 8 de junio de 2018

Meningitis - OMIM - NCBI

Meningitis - OMIM - NCBI

Meningitis

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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CAUDAL DYSGENESIS SYNDROME, INCLUDED
Cytogenetic locations: 1p13.1
19.
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A, INCLUDED
Cytogenetic locations: 1pter-p36.13, 13q13.3, 1pter-p36.13, 1q21.3

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