Co-Authors
This is a "connection" page, showing publications co-authored by REBECCA LITTLEJOHN and MELISSA STUEBBEN.
Connection Strength
0.114
-
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B. Am J Hum Genet. 2025 Nov 06; 112(11):2625-2642.
Score: 0.060
-
Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102.
Score: 0.054