Co-Authors
This is a "connection" page, showing publications co-authored by SCOTT MCLEAN and MELISSA STUEBBEN.
Connection Strength
0.174
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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. 2026 Mar 05; 113(3):636.
Score: 0.061
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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
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Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102.
Score: 0.054