Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus.
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| Description | scientific article published on 25 May 2012 |
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author: Saskia Lesnik Oberstein Yu Sun |
| Publication date | May 25, 2012 |
| Language | English |
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