Spranger, Stephanie

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

Horn, D., Kapeller, J., Rivera-Brugués, N., Moog, U., Lorenz-Depiereux, B., Eck, S., Hempel, M., Wagenstaller, J., Gawthrope, A., Monaco, A. P., et al. (2010) · Human Mutation

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Ehlers-Danlos Syndrome Type VII: Clinical Features and Molecular Defects*

GIUNTA, C., SUPERTI-FURGA, A., SPRANGER, S., COLE, W. G., & STEINMANN, B. (1999) · The Journal of Bone & Joint Surgery

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