Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: a case report and review of literature.
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| Description | scientific article published on 06 December 2013 |
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author: İbrahim Tanyalçın Kathelijn Keymolen Tim Vanderhasselt Anna C Jansen |
| Publication date | December 6, 2013 |
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