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Full Text	Issue Date	Title	Author(s)
	2011	A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani family	Basit, S.; Iqbal, Z.; Umicevic-Mirkov, M.; Kamran Ul-Hassan Naqvi, S.; Coenen, M.J.H.; Ansar, M.; Bokhoven, J.H.L.M. van; Ahmad, W.
	2010	Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.	Iqbal, Z.; Cejudo-Martin, P.; Brouwer, A.; Zwaag, B. van der; Ruiz-Lozano, P.; Scimia, M.C.; Lindsey, J.D.; Weinreb, R.; Albrecht, B.; Megarbane, A.; Alanay, Y.; Ben-Neriah, Z.; Amenduni, M.; Artuso, R.; Veltman, J.A.; Beusekom, E. van; Oudakker, A.R.; Millan, J.L.; Hennekam, R.; Hamel, B.C.J.; Courtneidge, S.A.; Bokhoven, J.H.L.M. van

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