Publications

Showing records 21 - 28 (of 28)

Publication: JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)

ID	Author	Year	Title	Publisher
1193605	Denora, Paola S; Schlesinger, David; Casali, Carlo; Kok, Fernando; Tessa, Alessandra; Boukhris, Amir; Azzedine, Hamid; Dotti, Maria Teresa; Bruno, Claudio; Truchetto, Jeremy; Biancheri, Roberta; Fedirko, Estelle; Di Rocco, Maja; Bueno, Clarissa; Malandrini, Alessandro; Battini, Roberta; Sickl, Elisabeth; de Leva, Maria Fulvia; Boespflug-Tanguy, Odile; Silvestri, Gabriella; Simonati, Alessandro; Said, Edith; Ferbert, Andreas; Criscuolo, Chiara; Heinimann, Karl; Modoni, Anna; Weber, Peter; Palmeri, Silvia; Plasilova, Martina; Pauri, Flavia; Cassandrini, Denise; Battisti, Carla; Pini, Antonella; Tosetti, Michela; Hauser, Erwin; Masciullo, Marcella; Di Fabio, Roberto; Piccolo, Francesca; Denis, Elodie; Cioni, Giovanni; Massa, Roberto; Della Giustina, Elvio; Calabrese, Olga; Melone, Marina A B; De Michele, Giuseppe; Federico, Antonio; Bertini, Enrico; Durr, Alexandra; Brockmann, Knut; van der Knaap, Marjo S; Zatz, Mayana; Filla, Alessandro; Brice, Alexis; Stevanin, Giovanni; Santorelli, Filippo M	2009	Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion	Human mutation : variations, databases, and diseases
1196145	Templeton, Arnoud; Marra, Giancarlo; Valtorta, Emanuele; Heinimann, Karl; Müller, Hansjakob; Köberle, Dieter; Gillessen, Silke	2009	Concordant colon tumors in monozygotic twins previously treated for prostate cancer	Familial cancer
1193020	Filges,Isabel; Röthlisberger,Benno; Noppen,Christoph; Boesch,Nemya; Wenzel,Friedel; Necker,Judith; Binkert,Franz; Huber,Andreas R; Heinimann,Karl; Miny,Peter	2009	Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33 : clinical and array-CGH study of a benign phenotype in a three-generation family	American journal of medical genetics
1194674	Filges, Isabel; Röthlisberger, Benno; Wenzel, Friedel; Heinimann, Karl; Huber, Andreas R; Miny, Peter	2008	Mosaic ring chromosome 8 : clinical and array-CGH findings in partial trisomy 8	American journal of medical genetics. Part A
1193970	Bujalkova, Maria; Zavodna, Katarina; Krivulcik, Tomas; Ilencikova, Denisa; Wolf, Brigitte; Kovac, Michal; Karner-Hanusch, Judith; Heinimann, Karl; Marra, Giancarlo; Jiricny, Josef; Bartosova, Zdena	2008	Multiplex SNaPshot genotyping for detecting loss of heterozygosity in the mismatch-repair genes MLH1 and MSH2 in microsatellite-unstable tumors	Clinical chemistry
1195332	Oliveira, J; Santos, R; Soares-Silva, I; Jorge, P; Vieira, E; Oliveira, M E; Moreira, A; Coelho, T; Ferreira, J C; Fonseca, M J; Barbosa, C; Prats, J; Aríztegui, M L; Martins, M L; Moreno, T; Heinimann, K; Barbot, C; Pascual-Pascual, S I; Cabral, A; Fineza, I; Santos, M; Bronze-da-Rocha, E	2008	LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients	Clinical genetics
1195322	Jaeger,E; Webb,E; Howarth,K; Carvajal-Carmona,L; Rowan,A; Broderick,P; Walther,A; Spain,S; Pittman,A; Kemp,Z; Sullivan,K; Heinimann,K; Lubbe,S; Domingo,E; Barclay,E; Martin,L; Gorman,M; Chandler,I; Vijayakrishnan,J; Wood,W; Papaemmanuil,E; Penegar,S; Qureshi,M; CORGI,Consortium; Farrington,S; Tenesa,A; Cazier,JB; Kerr,D; Gray,R; Peto,J; Dunlop,M; Campbell,H; Thomas,H; Houlston,R; Tomlinson,I	2008	Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk	Nature genetics

JournalItem (Kommentare, Editorials, Rezensionen, Urteilsanmerk., etc. in einer wissensch. Zeitschr.

ID	Author	Year	Title	Publisher
1197546	Ferrarini, Alessandra; Auteri-Kaczmarek, Agnes; Pica, Alessia; Boesch, Nemya; Heinimann, Karl; Schäfer, Stephan C; Vesnaver-Megalo, Sara; Cina, Viviane; Beckmann, Jacques S; Monnerat, Christian	2011	Early occurrence of lung adenocarcinoma and breast cancer after radiotherapy of a chest wall sarcoma in a patient with a de novo germline mutation in TP53	Familial cancer

Showing records 21 - 28 (of 28)