Number of items: 1.
2009
Lacbawan, F.,
Solomon, B. D.,
Roessler, E.,
El-Jaick, K. 
,
Domene, S.,
Velez, J. I. 
,
Zhou, N.,
Hadley, D.,
Balog, J. Z.,
Long, R.,
Fryer, A.,
Smith, W.,
Omar, S.,
McLean, S. D.,
Clarkson, K.,
Lichty, A.,
Clegg, N. J.,
Delgado, M. R.,
Levey, E.,
Stashinko, E.,
Potocki, L.,
VanAllen, M. I.,
Clayton-Smith, J.,
Donnai, D.,
Bianchi, D. W.,
Juliusson, P. B.,
Njolstad, P. R.,
Brunner, H. G.,
Carey, J. C.,
Hehr, U.,
Musebeck, J.,
Wieacker, P. F.,
Postra, A.,
Hennekam, R. C. M.,
van den Boogaard, M.-J. H.,
van Haeringen, A.,
Paulussen, A.,
Herbergs, J.,
Schrander-Stumpel, C. T. R. M.,
Janecke, A. R. 
,
Chitayat, D.,
Hahn, J.,
McDonald-McGinn, D. M.,
Zackai, E. H.,
Dobyns, W. B. 
and
Muenke, M. 
(2009)
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
Journal of Medical Genetics 46 (6), pp. 389-398.
Fulltext not available.
This list was generated on Tue May 20 19:20:01 2025 CEST.