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

✍ Scribed by Mitchel J. Pariani; Andrew Spencer; John M. Graham Jr.; David L. Rimoin


Book ID
116433179
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
429 KB
Volume
52
Category
Article
ISSN
1769-7212

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