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	1.	Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis. [electronic resource] by Perdu, B Lakeman, P Mortier, G Koenig, R Lachmeijer, A M A Van Hul, W Producer: 20130822 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes. [electronic resource] by Houweling, A C de Mooij, Y M van der Burgt, I Yntema, H G Lachmeijer, A M A Go, A T J I Producer: 20100608 In: Prenatal diagnosis vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly. [electronic resource] by Morris-Rosendahl, D J Najm, J Lachmeijer, A M A Sztriha, L Martins, M Kuechler, A Haug, V Zeschnigk, C Martin, P Santos, M Vasconcelos, C Omran, H Kraus, U Van der Knaap, M S Schuierer, G Kutsche, K Uyanik, G Producer: 20081215 In: Clinical genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. [electronic resource] by Revencu, N Boon, L M Dompmartin, A Rieu, P Busch, W L Dubois, J Forzano, F van Hagen, J M Halbach, S Kuechler, A Lachmeijer, A M A Lähde, J Russell, L Simola, K O J Mulliken, J B Vikkula, M Producer: 20130627 In: Molecular syndromology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)