Co-Authors
This is a "connection" page, showing publications co-authored by DARYL SCOTT and KEREN MACHOL.
Connection Strength
0.106
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A Rare Molecular Diagnosis in a Patient With Hepatocerebral Syndrome Contributes to the Expansion of the Phenotypic Spectrum of POLG2-Related Mitochondrial Disorder. Am J Med Genet A. 2025 Jul 09; e64177.
Score: 0.061
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Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans. Am J Med Genet A. 2021 03; 185(3):836-840.
Score: 0.045