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	1.	Induction of FAS ligand expression in a human hepatoblastoma cell line by HCV core protein. [electronic resource] by Ruggieri, A Murdolo, M Rapicetta, M Producer: 20040204 In: Virus research vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The terminal 760 kb region on 4p16 is unlikely to be the critical interval for growth delay in Wolf-Hirschhorn syndrome. [electronic resource] by Zollino, M Murdolo, M Neri, G Producer: 20080919 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cell cycle perturbation in a human hepatoblastoma cell line constitutively expressing Hepatitis C virus core protein. [electronic resource] by Ruggieri, A Murdolo, M Harada, T Miyamura, T Rapicetta, M Producer: 20040315 In: Archives of virology vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome. [electronic resource] by Jiraanont, P Hagerman, R J Neri, G Zollino, M Murdolo, M Tassone, F Producer: 20170202 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The first 4p euchromatic variant in a healthy carrier having an unusual reproductive history. [electronic resource] by Rodríguez, L Zollino, M Mansilla, E Martínez-Fernández, M L Pérez, P Murdolo, M Martínez-Frías, M L Producer: 20070713 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patients. [electronic resource] by Kavamura, M I Zollino, M Lecce, R Murdolo, M Brunoni, D Alchorne, M M A Opitz, J M Neri, G Producer: 20040130 In: American journal of medical genetics. Part A vol. 119A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome. [electronic resource] by Kavamura, M I Pomponi, M G Zollino, M Lecce, R Murdolo, M Brunoni, D Alchorne, M M A Opitz, J M Neri, G Producer: 20030826 In: European journal of human genetics : EJHG vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)