Co-Authors
This is a "connection" page, showing publications co-authored by SHWETA DHAR and SEEMA LALANI.
Connection Strength
0.088
-
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar 07.
Score: 0.062
-
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell. 2011 Sep 16; 146(6):889-903.
Score: 0.026