A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis

Authors

Keywords

Journal

Volume 52, Issue 2-3, Pages 123-127

Publisher

Elsevier BV

Online

2009-03-31

DOI

10.1016/j.ejmg.2009.03.012

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