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	1.	Heterogeneity in the origin of recurrent complete hydatidiform moles: not all women with multiple molar pregnancies have biparental moles. [electronic resource] by van der Smagt, J J Scheenjes, E Kremer, J A M Hennekam, F A M Fisher, R A Producer: 20060713 In: BJOG : an international journal of obstetrics and gynaecology vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Age of mother and grandmother in relation to a subject's breast cancer risk. [electronic resource] by de Haan, M C Michels, K B Peeters, P H M van Noord, P A H Hennekam, F A M van der Schouw, Y T Producer: 20100528 In: British journal of cancer vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population. [electronic resource] by Verbeek, Dineke S Warrenburg, Bart P C van de Hennekam, F A M Dooijes, Dennis Ippel, P F Verschuuren-Bemelmans, Corien C Kremer, H P H Sinke, Richard J Producer: 20050719 In: Human genetics vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family. [electronic resource] by van de Warrenburg, B P C Verbeek, D S Piersma, S J Hennekam, F A M Pearson, P L Knoers, N V A M Kremer, H P H Sinke, R J Producer: 20040203 In: Neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients. [electronic resource] by Letteboer, T G W Zewald, R A Kamping, E J de Haas, G Mager, J J Snijder, R J Lindhout, D Hennekam, F A M Westermann, C J J Ploos van Amstel, J K Producer: 20050421 In: Human genetics vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation. [electronic resource] by van der Smagt, Jasper J van der Zwaag, Paul A van Tintelen, J Peter Cox, Moniek G P J Wilde, Arthur A M van Langen, Irene M Ummels, Amber Hennekam, F A M Dooijes, Dennis Gerbens, Frans Bikker, Hennie Hauer, Richard N W Doevendans, Pieter A Producer: 20130506 In: Cardiology vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)