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	1.	A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2. [electronic resource] by Kevelam, Sietske H G van Harssel, Jeske J T van der Zwaag, Bert Smeets, Hubertus J M Paulussen, Aimee D C Lichtenbelt, Klaske D Producer: 20130620 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	No Fabry Disease in Patients Presenting with Isolated Small Fiber Neuropathy. [electronic resource] by de Greef, Bianca T A Hoeijmakers, Janneke G J Wolters, Emma E Smeets, Hubertus J M van den Wijngaard, Arthur Merkies, Ingemar S J Faber, Catharina G Gerrits, Monique M Producer: 20160724 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Yield of peripheral sodium channels gene screening in pure small fibre neuropathy. [electronic resource] by Eijkenboom, Ivo Sopacua, Maurice Hoeijmakers, Janneke G J de Greef, Bianca T A Lindsey, Patrick Almomani, Rowida Marchi, Margherita Vanoevelen, Jo Smeets, Hubertus J M Waxman, Stephen G Lauria, Giuseppe Merkies, Ingemar S J Faber, Catharina G Gerrits, Monique M Producer: 20191209 In: Journal of neurology, neurosurgery, and psychiatry vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)