Waisman Center
Advancing knowledge of human development, developmental disabilities, and neurodegenerative diseases.

Phenotype of FOXP2 haploinsufficiency in a mother and son

Phenotype of FOXP2 Haploinsufficiency in a Mother and Son.

Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD. (2012) Phenotype of FOXP2 haploinsufficiency in a mother and son. American Journal of Medical Genetics: Part A. 158A(1):174-81.