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Functional characterization of two enhancers located downstream FOXP2.
BMC Med Genet. 2019 May 2;20(1):65. doi: 10.1186/s12881-019-0810-2.
BMC Med Genet. 2019.
PMID: 31046704
Free PMC article.
Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.
Moralli D, Nudel R, Chan MT, Green CM, Volpi EV, Benítez-Burraco A, Newbury DF, García-Bellido P.
Moralli D, et al. Among authors: garcia bellido p.
Mol Cytogenet. 2015 Jun 10;8:36. doi: 10.1186/s13039-015-0148-1. eCollection 2015.
Mol Cytogenet. 2015.
PMID: 26060509
Free PMC article.
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Human-specific changes in two functional enhancers of FOXP2.
Benítez-Burraco A, Torres-Ruiz R, Gelabert P, Lalueza-Fox C, Rodríguez-Perales S, García-Bellido P.
Benítez-Burraco A, et al. Among authors: garcia bellido p.
Cell Mol Biol (Noisy-le-grand). 2022 Nov 30;68(11):16-19. doi: 10.14715/cmb/2022.68.11.3.
Cell Mol Biol (Noisy-le-grand). 2022.
PMID: 37114314
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