domingo, 20 de mayo de 2018

Neurofibromatosis - OMIM - NCBI

Neurofibromatosis - OMIM - NCBI

Neurofibromatosis

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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NF1 MICRODUPLICATION SYNDROME, INCLUDED
Cytogenetic locations: 17q11.2
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