Publications by authors named "David Matthes"

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Identification of a de novo FOXP1 mutation and incidental discovery of inherited genetic variants contributing to a case of autism spectrum disorder and epilepsy.
Kristy Jay, Amit Mitra, Taylor Harding, David Matthes, Brian Van Ness

Mol Genet Genomic Med· July 2019

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IBI series winner. Students propose genetic solutions to societal problems.
Sue Wick, Mark Decker, David Matthes, Robin Wright

Science· September 2013

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Semaphorin 4A is dynamically regulated during thymocyte development in mice.
Grace E Linder, Pavlina D Chuntova, Bryce T McLelland, Leonor Añó, Udochukwu C Obodo, David J Matthes

Cell Immunol· February 2013

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