Further delineation of the phenotype of chromosome 14q13...

Journal of Medical Genetics 2012 / 06 Vol. 49; Iss. 6

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

Santen, G. W. E., Sun, Y., Gijsbers, A. C. J., Carre, A., Holvoet, M., Haeringen, A. v., Lesnik Oberstein, S. A. J., Tomoda, A., Mabe, H., Polak, M., Devriendt, K., Ruivenkamp, C. A. L., Bijlsma, E. K
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Volume:
49
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2011-100721
Date:
June, 2012
File:
PDF, 384 KB
english, 2012
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