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Author/Creator Muenke, M

2. 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) ↗

5. Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. Issue 2 (17th June 2005)

Authors:
Van Maldergem, L; Siitonen, H A; Jalkh, N; Chouery, E; De Roy, M; Delague, V; Muenke, M; Jabs, E W; Cai, J; Wang, L L; Plon, S E; Fourneau, C; Kestilä, M; Gillerot, Y; Mégarbané, A; Verloes, A
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 2(2006)
Page Start:
148
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗