Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
- DOI
- 10.1002/humu.21362
- Published
- 2010 Nov
- Container
- Human mutation
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/humu.21362,
title = {Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.},
author = {Horn D and Kapeller J and Rivera-Brugués N and Moog U and Lorenz-Depiereux B and Eck S and Hempel M and Wagenstaller J and Gawthrope A and Monaco AP and Bonin M and Riess O and Wohlleber E and Illig T and Bezzina CR and Franke A and Spranger S and Villavicencio-Lorini P and Seifert W and Rosenfeld J and Klopocki E and Rappold GA and Strom TM},
year = {2010},
journal = {Human mutation},
doi = {10.1002/humu.21362},
url = {https://doi.org/10.1002/humu.21362}
}RIS
TY - JOUR TI - Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. AU - Horn D AU - Kapeller J AU - Rivera-Brugués N AU - Moog U AU - Lorenz-Depiereux B AU - Eck S AU - Hempel M AU - Wagenstaller J AU - Gawthrope A AU - Monaco AP AU - Bonin M AU - Riess O AU - Wohlleber E AU - Illig T AU - Bezzina CR AU - Franke A AU - Spranger S AU - Villavicencio-Lorini P AU - Seifert W AU - Rosenfeld J AU - Klopocki E AU - Rappold GA AU - Strom TM PY - 2010 JO - Human mutation DO - 10.1002/humu.21362 UR - https://doi.org/10.1002/humu.21362 ER -
APA
D, H., J, K., N, R., U, M., B, L., S, E., M, H., J, W., A, G., AP, M., M, B., O, R., E, W., T, I., CR, B., A, F., S, S., P, V., W, S., J, R., E, K., GA, R., & TM, S. (2010). Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.. Human mutation. https://doi.org/10.1002/humu.21362
Source records
- pubmed · retrieved 2026-09-25T08:02:28.059Z