Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays.

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Published in Hum Mutat on August 13, 2013

Authors

Andrey Shuvarikov1, Ian M Campbell, Piotr Dittwald, Nicholas J Neill, Martin G Bialer, Christine Moore, Patricia G Wheeler, Stephanie E Wallace, Mark C Hannibal, Michael F Murray, Monica A Giovanni, Deborah Terespolsky, Sandi Sodhi, Matteo Cassina, David Viskochil, Billur Moghaddam, Kristin Herman, Chester W Brown, Christine R Beck, Anna Gambin, Sau Wai Cheung, Ankita Patel, Allen N Lamb, Lisa G Shaffer, Jay W Ellison, J Britt Ravnan, Paweł Stankiewicz, Jill A Rosenfeld

Author Affiliations

1: Signature Genomic Laboratories, PerkinElmer, Inc, Spokane, Washington.

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