Connection | Profiles RNS

Search Result Details

Back to Search Results

This page shows the details of why an item matched the keywords from your search.

Search Results

Das, Soma

One or more keywords matched the following items that are connected to Das, Soma

Item Type	Name
Concept	Comparative Genomic Hybridization
Academic Article	The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
Academic Article	Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing.
Academic Article	Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome.

Search Criteria