Eden Haverfield to Sequence Analysis, DNA
This is a "connection" page, showing publications Eden Haverfield has written about Sequence Analysis, DNA.
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Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. Am J Med Genet A. 2016 07; 170(7):1791-8.
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Clinical application of whole-exome sequencing across clinical indications. Genet Med. 2016 07; 18(7):696-704.
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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. Am J Hum Genet. 2015 Aug 06; 97(2):343-52.
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Molecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally. Prenat Diagn. 2014 Feb; 34(2):163-7.
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