A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
- 28 March 2009
- journal article
- case report
- Published by Elsevier BV in European Journal of Medical Genetics
- Vol. 52 (2-3), 123-127
- https://doi.org/10.1016/j.ejmg.2009.03.012
Abstract
No abstract availableKeywords
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