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![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](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
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
- All authors
- Santen, G.W.E.; Sun, Y.; Gijsbers, A.C.J.; Carre, A.; Holvoet, M.; Haeringen, A. van; Oberstein, S.A.J.L.; Tomoda, A.; Mabe, H.; Polak, M.; Devriendt, K.; Ruivenkamp, C.A.L.; Bijlsma, E.K.
- Date
- 2012-06-28
- Journal
- Journal of Medical Genetics
- Volume
- 49
- Issue
- 6
- Pages
- 366 - 72