DANIEL PENNY to Phenotype
This is a "connection" page, showing publications DANIEL PENNY has written about Phenotype.
Connection Strength
0.045
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Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise. Heart Rhythm. 2018 07; 15(7):1042-1050.
Score: 0.017
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Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals. Circ Arrhythm Electrophysiol. 2017 Apr; 10(4).
Score: 0.016
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Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome. Am J Med Genet A. 2013 Sep; 161A(9):2305-10.
Score: 0.012