1. Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. Issue 6 (2nd April 2009) Authors: Lacbawan, F; Solomon, B D; Roessler, E; El-Jaick, K; Domené, S; Vélez, 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 Journal: Journal of medical genetics Issue: Volume 46:Issue 6(2009) Page Start: 389 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia. Issue 5 (30th April 2004) Authors: Wieland, I; Muschke, P; Jakubiczka, S; Volleth, M; Freigang, B; Wieacker, P F Journal: Journal of medical genetics Issue: Volume 41:Issue 5(2004) Page Start: e54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗