Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects von de Wit, M C Y, Kros, J M, Halley, D J J, de Coo, I F M, Verdijk, R, Jacobs, B C, Mancini, G M S

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Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-d... von Hes, FJ, van der Luijt, RB, Janssen, ALW, Zewald, RA, de Jong, GJ, Lenders, JW, Links, TP, Luyten, GPM, Sijmons, RH, Eussen, HJ, Halley, DJJ, Lips, CJM, Pearson, PL, van den Ouweland, AMW, Majoor-Krakauer, DF

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The beaver's reconquest of Eurasia: status, population development and management of a conservation success von HALLEY, D. J., ROSELL, F.

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Movement disorder and neuronal migration disorder due to ARFGEF2 mutation von de Wit, M. C. Y., de Coo, I. F. M., Halley, D. J. J., Lequin, M. H., Mancini, G. M. S.

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A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands von van Minkelen, R., van Bever, Y., Kromosoeto, J.N.R., Withagen-Hermans, C.J., Nieuwlaat, A., Halley, D.J.J., van den Ouweland, A.M.W.

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Diet: tissue stable isotope fractionation of carbon and nitrogen in blood plasma and whole blood of male reindeer Rangifer tarandus von Halley, D. J, Minagawa, M, Nieminen, M, Gaare, E

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Broad spectrum of Pompe disease in patients with the same c.-32-13T→G haplotype von KROOS, M. A, POMPONIO, R. J, HALLEY, D. J. J, VAN DER PLOEG, A. T, REUSER, A. J. J, HAGEMANS, M. L, KEULEMANS, J. L. M, PHIPPS, M, DERISO, M, PALMER, R. E, AUSEMS, M. G. E. M, VAN DER BEEK, N. A. M. E, VAN DIGGELEN, O. P

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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings von Bronsveld, I, Mekus, F, Bijman, J, Ballmann, M, de Jonge, H R, Laabs, U, Halley, D J, Ellemunter, H, Mastella, G, Thomas, S, Veeze, H J, Tümmler, B

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Excavation and architecture of Argentine ant nests von HALLEY, J. D, BURD, M, WELLS, P

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Genetic risk factors in infertile men with severe oligozoospermia and azoospermia von Dohle, G.R., Halley, D.J.J., Van Hemel, J.O., van den Ouwel, A.M.W., Pieters, M.H.E.C., Weber, R.F.A., Govaerts, L.C.P.

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The spectrum of mutations in UBE3A causing Angelman syndrome von PING FANG, LEV-LEHMAN, E, LANGLOIS, S, GRAHAM, J. M, BEUTEN, J, WILLEMS, P. J, LEDBETTER, D. H, BEAUDET, A. L, TSAI, T.-F, MATSUURA, T, BENTON, C. S, SUTCLIFFE, J. S, CHRISTIAN, S. L, KUBOTA, T, HALLEY, D. J, MEIJERS-HEIJBOER, H

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Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood von VERHOEF, S, VAN DIEMEN-STEENVOORDE, R, LIPS, K, VAN DEN OUWELAND, A. M. W, AKKERSDIJK, W. L, BAX, N. M. A, ARIYUREK, Y, HERMANS, C. J, VAN NIEUWENHUIZEN, O, NIKKELS, P. G. J, LINDHOUT, D, HALLEY, D. J. J

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Mental status of females with an FMR1 gene full mutation von DE VRIES, B. B. A, WIEGERS, A. M, NIERMEIJER, M. F, SMITS, A. P. T, MOHKAMSING, S, DUIVENVOORDEN, H. J, FRYNS, J.-P, CURFS, L. M. G, HALLEY, D. J. J, OOSTRA, B. A, VAN DEN OUWELAND, A. M. W

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Nonequilibrium dynamics of social groups: insights from foraging Argentine ants von HALLEY, J. D, BURD, M

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Plant traits link hypothesis about resource-use and response to herbivory von Rusch, G.M., Skarpe, C., Halley, D.J.

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Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuber von JANSEN, F. E, NOTENBOOM, R. G. E, NELLIST, M, GOEDBLOED, M. A, HALLEY, D. J, DE GRAAN, P. N. E, VAN NIEUWENHUIZEN, O

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A prospective 10 year follow up study of patients with neurofibromatosis type 1 von Cnossen, M H, de Goede-Bolder, A, van den Broek, K M, Waasdorp, C M E, Oranje, A P, Stroink, H, Simonsz, H J, van den Ouweland, A M W, Halley, D J J, Niermeijer, M F

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A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting von Ramsoekh, D, Wagner, A, van Leerdam, M E, Dinjens, W N M, Steyerberg, E W, Halley, D J J, Kuipers, E J, Dooijes, D

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Common C-to-T Substitution at Position -480 of the Hepatic Lipase Promoter Associated With a Lowered Lipase Activity in Coronary Artery Disease Patients von Jansen, Hans, Verhoeven, Adrie J.M, Weeks, Lilian, Kastelein, John J.P, Halley, Dicky J.J, van den Ouweland, Ans, Jukema, J. Wouter, Seidell, Jaap C, Birkenhager, Jan C

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Survival in Hereditary Breast Cancer Associated With Germline Mutations of BRCA2 von VERHOOG, L. C, BREKELMANS, C. T. M, VAN DEN OUWELAND, A. M. W, MEIJERS-HEIJBOER, E. J, KLIJN, J. G. M, SEYNAEVE, C, DAHMEN, G, VAN GEEL, A. N, BARTELS, C. C. M, TILANUS-LINTHORST, M. M. A, WAGNER, A, DEVILEE, P, HALLEY, D. J. J

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