Co-Authors
This is a "connection" page, showing publications co-authored by CHAYA MURALI and HALEY STREFF.
Connection Strength
0.533
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A familial deletion of 10p12.1 associated with thrombocytopenia. Am J Med Genet A. 2024 Jan; 194(1):77-81.
Score: 0.240
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A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome. Am J Med Genet A. 2023 06; 191(6):1576-1580.
Score: 0.231
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Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 Feb 28; 101102.
Score: 0.062