ELIZABETH ROEDER to INDEL Mutation
This is a "connection" page, showing publications ELIZABETH ROEDER has written about INDEL Mutation.
Connection Strength
0.156
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De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome Med. 2019 02 28; 11(1):12.
Score: 0.156