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    Lonjou, C., Eon‐Marchais, S., Truong, T., Dondon, M., Karimi, M., Jiao, Y., Damiola, F., Barjhoux, L., Le Gal, D., Beauvallet, J., Mebirouk, N., Cavaciuti, E., Chiesa, J., Floquet, A., Audebert‐Bellanger, S., Giraud, S., Frebourg, T., Limacher, J., Gladieff, L., Mortemousque, I., Dreyfus, H., Lejeune‐Dumoulin, S., Lasset, C., Venat‐Bouvet, L., Bignon, Y., Pujol, P., Maugard, C. M., Luporsi, E., Bonadona, V., Noguès, C., Berthet, P., Delnatte, C., Gesta, P., Lortholary, A., Faivre, L., Buecher, B., Caron, O., Gauthier‐Villars, M., Coupier, I., Mazoyer, S., Monraz, L., Kondratova, M., Kuperstein, I., Guénel, P., Barillot, E., Stoppa‐Lyonnet, D., Andrieu, N., & Lesueur, F. (2021). gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility. International journal of cancer, 148(8), 1895–1909. http://access.bl.uk/ark:/81055/vdc_100122905427.0x000059
  
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