Article info
PDFCopy-number variation
Original article
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
- Correspondence to Dr Gijs W E Santen, Center for Human and Clinical Genetics, Leiden University Medical Center (LUMC), Albinusdreef 2, Postbus 9600, Leiden 2300 RC, The Netherlands; santen{at}lumc.nl
Citation
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
Publication history
- Received February 9, 2012
- Accepted April 2, 2012
- First published May 25, 2012.
Online issue publication
April 27, 2016
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- Previous version (27 April 2016).
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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.