Co-Authors
This is a "connection" page, showing publications co-authored by Kenton Holden and Maria Matheus.
Connection Strength
0.681
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Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies. J Child Neurol. 2015 Oct; 30(12):1664-8.
Score: 0.514
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Importance of genetic testing in global health during the evaluation of familial microcephaly. Clin Case Rep. 2016 10; 4(10):968-971.
Score: 0.141
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LIS1 duplication: expanding the phenotype. J Child Neurol. 2012 Jun; 27(6):791-5.
Score: 0.025