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Browsing by Author Duyvenvoorde, H.A. van
Showing results 1 to 6 of 6
| Full Text | Issue Date | Title | Author(s) | | 2011 | The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated protein | Duyvenvoorde, H.A. van; Doorn, J. van; Koenig, J.; Gauguin, L.; Oostdijk, W., et al |
| 2011 | Case report: low circulating IGF-I levels due to Acid-Labile Subunit deficiency in adulthood are not associated with early development of atherosclerosis and impaired heart function | Rensing, K.L.; Duyvenvoorde, H.A. van; Cramer, M.J.; Teske, A.J.; Prokop, M., et al |
| 2010 | Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 gene. | Duyvenvoorde, H.A. van; Setten, P.A. van; Walenkamp, M.J.; Doorn, J. van; Koenig, J., et al |
| 2009 | Human acid-labile subunit deficiency: clinical, endocrine and metabolic consequences. | Domene, H.M.; Hwa, V.; Argente, J.; Wit, J.M.; Camacho-Hubner, C., et al |
| 2008 | Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. | Bon, B.W.M. van; Koolen, D.A.; Borgatti, R.; Magee, A.; Garcia-Minaur, S., et al |
| 2008 | Homozygous and heterozygous expression of a novel mutation of the acid-labile subunit. | Duyvenvoorde, H.A. van; Kempers, M.J.E.; Twickler, T.B.; Doorn, J. van; Gerver, W.J., et al |
Showing results 1 to 6 of 6
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