Publications by authors named "Katherine D Rutledge"

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Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.
Fady M Mikhail, Edward J Lose, Nathaniel H Robin, Maria D Descartes, Katherine D Rutledge, S Lane Rutledge

Am J Med Genet A· October 2011

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IRF6 mutations in mixed isolated familial clefting.
Katherine D Rutledge, Christina Barger, John H Grant, Nathaniel H Robin

Am J Med Genet A· December 2010

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Further delineation of the Kapur-Toriello syndrome.
Nathaniel H Robin, Katherine D Rutledge, Peter D Ray, John H Grant

Am J Med Genet A· April 2010

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Imperforate anus is a rare associated finding in blepharocheilodontic syndrome.
K Nicole Weaver, Katherine D Rutledge, John H Grant, Nathaniel H Robin

Am J Med Genet A· February 2010

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