LINDSAY BURRAGE to Craniofacial Abnormalities
This is a "connection" page, showing publications LINDSAY BURRAGE has written about Craniofacial Abnormalities.
Connection Strength
0.220
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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: 0.130
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The genetic basis of DOORS syndrome: an exome-sequencing study. Lancet Neurol. 2014 Jan; 13(1):44-58.
Score: 0.090