The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
- DOI
- 10.1136/jmg.2010.087528
- Published
- 2011 Jun
- Container
- Journal of medical genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1136/jmg.2010.087528,
title = {The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.},
author = {Kortüm F and Das S and Flindt M and Morris-Rosendahl DJ and Stefanova I and Goldstein A and Horn D and Klopocki E and Kluger G and Martin P and Rauch A and Roumer A and Saitta S and Walsh LE and Wieczorek D and Uyanik G and Kutsche K and Dobyns WB},
year = {2011},
journal = {Journal of medical genetics},
doi = {10.1136/jmg.2010.087528},
url = {https://doi.org/10.1136/jmg.2010.087528}
}RIS
TY - JOUR TI - The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. AU - Kortüm F AU - Das S AU - Flindt M AU - Morris-Rosendahl DJ AU - Stefanova I AU - Goldstein A AU - Horn D AU - Klopocki E AU - Kluger G AU - Martin P AU - Rauch A AU - Roumer A AU - Saitta S AU - Walsh LE AU - Wieczorek D AU - Uyanik G AU - Kutsche K AU - Dobyns WB PY - 2011 JO - Journal of medical genetics DO - 10.1136/jmg.2010.087528 UR - https://doi.org/10.1136/jmg.2010.087528 ER -
APA
F, K., S, D., M, F., DJ, M., I, S., A, G., D, H., E, K., G, K., P, M., A, R., A, R., S, S., LE, W., D, W., G, U., K, K., & WB, D. (2011). The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.. Journal of medical genetics. https://doi.org/10.1136/jmg.2010.087528
Source records
- pubmed · retrieved 2026-09-25T13:31:39.004Z