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	1.	Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism. [electronic resource] by Trevisson, E Forzan, M Salviati, L Clementi, M Producer: 20150512 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Dysfunctional coping is related to impaired skin-related quality of life and psychological distress in patients with neurofibromatosis type 1 with major skin involvement. [electronic resource] by Bottesi, G Spoto, A Trevisson, E Zuccarello, D Vidotto, G Cassina, M Clementi, M Producer: 20210514 In: The British journal of dermatology vol. 182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Osteopathia striata with cranial sclerosis and Wilms tumor: Coincidence or consequence? [electronic resource] by Sperotto, F Bisogno, G Opocher, E Rossi, S Rigon, C Trevisson, E Mercolini, F Producer: 20190424 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Numerical activities of daily living in adults with neurofibromatosis type 1. [electronic resource] by Burgio, F Benavides-Varela, S Arcara, G Trevisson, E Frizziero, D Clementi, M Semenza, C Producer: 20180604 In: Journal of intellectual disability research : JIDR vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants. [electronic resource] by Gigante, M Diella, S Santangelo, L Trevisson, E Acosta, M J Amatruda, M Finzi, G Caridi, G Murer, L Accetturo, M Ranieri, E Ghiggeri, G M Giordano, M Grandaliano, G Salviati, L Gesualdo, L Producer: 20190415 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Alport syndrome: impact of digenic inheritance in patients management. [electronic resource] by Fallerini, C Baldassarri, M Trevisson, E Morbidoni, V La Manna, A Lazzarin, R Pasini, A Barbano, G Pinciaroli, A R Garosi, G Frullanti, E Pinto, A M Mencarelli, M A Mari, F Renieri, A Ariani, F Producer: 20180316 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)