Co-Authors
This is a "connection" page, showing publications co-authored by SHWETA DHAR and LISA EMRICK.
Connection Strength
0.108
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Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar 07.
Score: 0.062
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Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun. 2019 10 15; 10(1):4679.
Score: 0.046