Genetic Abnormalities inFOXP1Are Associated with Congenital Heart Defects

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Modifying Mendel

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3p Interstitial Deletion

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Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

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Left Ventricular Hypoplasia

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Loss-of-function mutation in GATA4 causes anomalies of human testicular development

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Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

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Foxp1 coordinates cardiomyocyte proliferation through both cell-autonomous and nonautonomous mechanisms

(2010) Y. Zhang et al.   GENES & DEVELOPMENT

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

(2010) Denise Horn et al.   HUMAN MUTATION

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

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Nkx2.7 and Nkx2.5 Function Redundantly and Are Required for Cardiac Morphogenesis of Zebrafish Embryos

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Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

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