LINDSAY BURRAGE to Abnormalities, Multiple
This is a "connection" page, showing publications LINDSAY BURRAGE has written about Abnormalities, Multiple.
Connection Strength
0.436
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LONP1 Variants Are Associated With Clinically Diverse Phenotypes. Clin Genet. 2026 Mar; 109(3):437-457.
Score: 0.152
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Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 9 affected individuals. Genet Med. 2019 01; 21(1):233-242.
Score: 0.092
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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features. Am J Hum Genet. 2017 Apr 06; 100(4):676-688.
Score: 0.085
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Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):579-83.
Score: 0.071
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Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. Am J Med Genet A. 2025 01; 197(1):e63845.
Score: 0.035