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	1.	Correction to: Reassessing the clinical spectrum associated with Hereditary Leiomyomatosis and Renal Cell Carcinoma syndrome in French FH mutation carriers. [electronic resource] by Muller, M Guillaud-Bataille, M Richard, S Benusiglio, P R Publication details: Clinical genetics 05 2018 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Isolated cutaneous leiomyosarcoma revealing a novel germline mutation of the fumarate hydratase gene. [electronic resource] by Weiler, L Poulalhon, N Slama, A Guillaud-Bataille, M Thomas, L Producer: 20170911 In: The British journal of dermatology vol. 175 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation. [electronic resource] by Bernheim, A Toujani, S Guillaud-Bataille, M Richon, C Waxin, H Dessen, P Berger, R Producer: 20080221 In: Cytogenetic and genome research vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Two populations of double minute chromosomes harbor distinct amplicons, the MYC locus at 8q24.2 and a 0.43-Mb region at 14q24.1, in the SW613-S human carcinoma cell line. [electronic resource] by Guillaud-Bataille, M Brison, O Danglot, G Lavialle, C Raynal, B Lazar, V Dessen, P Bernheim, A Producer: 20090519 In: Cytogenetic and genome research vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system. [electronic resource] by Inda, M M Perot, C Guillaud-Bataille, M Danglot, G Rey, J A Bello, M J Fan, X Eberhart, C Zazpe, I Portillo, E Tuñón, T Martínez-Peñuela, J M Bernheim, A Castresana, J S Producer: 20060126 In: Histopathology vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Screening in asymptomatic SDHx mutation carriers: added value of ¹⁸F-FDG PET/CT at initial diagnosis and 1-year follow-up. [electronic resource] by Lepoutre-Lussey, C Caramella, C Bidault, F Déandreis, D Berdelou, A Al Ghuzlan, A Hartl, D Borget, I Gimenez-Roqueplo, A-P Dumont, F Deschamps, F Nascimento, C Lumbroso, J Guillaud Bataille, M Schlumberger, M Baudin, E Leboulleux, S Producer: 20151222 In: European journal of nuclear medicine and molecular imaging vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers. [electronic resource] by Muller, M Ferlicot, S Guillaud-Bataille, M Le Teuff, G Genestie, C Deveaux, S Slama, A Poulalhon, N Escudier, B Albiges, L Soufir, N Avril, M-F Gardie, B Saldana, C Allory, Y Gimenez-Roqueplo, A-P Bressac-de Paillerets, B Richard, S Benusiglio, P R Producer: 20180703 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)