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Osteosarcoma without prior retinoblastoma related to RB1 low‐penetrance germline pathogenic variants: A novel type of RB1‐related hereditary predisposition syndrome?
Published in:
Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 12, p. N.PAG, doi. 10.1002/mgg3.913
By:
- Imbert‐Bouteille, Marion;
- Gauthier‐Villars, Marion;
- Leroux, Dominique;
- Meunier, Isabelle;
- Aerts, Isabelle;
- Lumbroso‐Le Rouic, Livia;
- Lejeune, Sophie;
- Delnatte, Capucine;
- Abadie, Caroline;
- Pujol, Pascal;
- Houdayer, Claude;
- Corsini, Carole
Publication type:
Article
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Published in:
2021
By:
- Ribeiro Guerra, Maximiliano;
- Coignard, Juliette;
- Eon-Marchais, Séverine;
- Dondon, Marie-Gabrielle;
- Le Gal, Dorothée;
- Beauvallet, Juana;
- Mebirouk, Noura;
- Belotti, Muriel;
- Caron, Olivier;
- Gauthier-Villars, Marion;
- Coupier, Isabelle;
- Buecher, Bruno;
- Lortholary, Alain;
- Fricker, Jean-Pierre;
- Gesta, Paul;
- Noguès, Catherine;
- Faivre, Laurence;
- Berthet, Pascaline;
- Luporsi, Elisabeth;
- Delnatte, Capucine
Publication type:
journal article
5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints.
Published in:
Cancers, 2021, v. 13, n. 13, p. 3171, doi. 10.3390/cancers13133171
By:
- Caputo, Sandrine M.;
- Telly, Dominique;
- Briaux, Adrien;
- Sesen, Julie;
- Ceppi, Maurizio;
- Bonnet, Françoise;
- Bourdon, Violaine;
- Coulet, Florence;
- Castera, Laurent;
- Delnatte, Capucine;
- Hardouin, Agnès;
- Mazoyer, Sylvie;
- Schultz, Inès;
- Sevenet, Nicolas;
- Uhrhammer, Nancy;
- Bonnet, Céline;
- Tilkin-Mariamé, Anne-Françoise;
- Houdayer, Claude;
- Moncoutier, Virginie;
- Andrieu, Catherine
Publication type:
Article
Mutation analysis of PALB2 gene in French breast cancer families.
Published in:
Breast Cancer Research & Treatment, 2015, v. 154, n. 3, p. 463, doi. 10.1007/s10549-015-3625-7
By:
- Damiola, Francesca;
- Schultz, Inès;
- Barjhoux, Laure;
- Sornin, Valérie;
- Dondon, Marie-Gabrielle;
- Eon-Marchais, Séverine;
- Marcou, Morgane;
- Caron, Olivier;
- Gauthier-Villars, Marion;
- Pauw, Antoine;
- Luporsi, Elisabeth;
- Berthet, Pascaline;
- Delnatte, Capucine;
- Bonadona, Valérie;
- Maugard, Christine;
- Pujol, Pascal;
- Lasset, Christine;
- Longy, Michel;
- Bignon, Yves-Jean;
- Fricker, Jean-Pierre
Publication type:
Article
Gestational choriocarcinoma associated with a germline TP53 mutation.
Published in:
Familial Cancer, 2018, v. 17, n. 1, p. 113, doi. 10.1007/s10689-017-9996-7
By:
- Brehin, Anne-Claire;
- Patrier-Sallebert, Sophie;
- Bougeard, Gaëlle;
- Side-Pfennig, Gwendoline;
- Llamas Gutierrez, Francisco;
- Lamy, Aude;
- Colasse, Elodie;
- Kandel-Aznar, Christine;
- Delnatte, Capucine;
- Vuillemin, Eric;
- Sadot-Lebouvier, Sophie;
- Odent, Sylvie;
- Sabourin, Jean-Christophe;
- Golfier, François;
- Frebourg, Thierry
Publication type:
Article
Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/ 2 mutations carriers: the LIBER trial.
Published in:
Familial Cancer, 2012, v. 11, n. 1, p. 77, doi. 10.1007/s10689-011-9484-4
By:
- Pujol, Pascal;
- Lasset, Christine;
- Berthet, Pascaline;
- Dugast, Catherine;
- Delaloge, Suzette;
- Fricker, Jean-Pierre;
- Tennevet, Isabelle;
- Chabbert-Buffet, Nathalie;
- This, Pascale;
- Baudry, Karen;
- Lemonnier, Jerome;
- Roca, Lise;
- Mijonnet, Sylvie;
- Gesta, Paul;
- Chiesa, Jean;
- Dreyfus, Helene;
- Vennin, Philippe;
- Delnatte, Capucine;
- Bignon, Yves;
- Lortholary, Alain
Publication type:
Article

Found: 6

Osteosarcoma without prior retinoblastoma related to RB1 low‐penetrance germline pathogenic variants: A novel type of RB1‐related hereditary predisposition syndrome?

Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.

5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints.

Mutation analysis of PALB2 gene in French breast cancer families.

Gestational choriocarcinoma associated with a germline TP53 mutation.

Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/ 2 mutations carriers: the LIBER trial.