Integrative Genetic Characterization and Phenotype Correlations in Pheochromocytoma and Paraganglioma Tumours

Por Crona, Joakim, Nordling, Margareta, Maharjan, Rajani, Granberg, Dan, Stålberg, Peter, Hellman, Per, Björklund, Peyman
Publicado em 2014

No germline mutations in supposed tumour suppressor genes SAFB1 and SAFB2 in familial breast cancer with linkage to 19p

Por Bergman, Annika, Abel, Frida, Behboudi, Afrouz, Yhr, Maria, Mattsson, Jan, Svensson, Jan H, Karlsson, Per, Nordling, Margareta
Publicado em 2008

A mutation in POLE predisposing to a multi-tumour phenotype

Por ROHLIN, ANNA, ZAGORAS, THEOFANIS, NILSSON, STAFFAN, LUNDSTAM, ULF, WAHLSTRÖM, JAN, HULTÉN, LEIF, MARTINSSON, TOMMY, KARLSSON, GÖRAN B., NORDLING, MARGARETA
Publicado em 2014

Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families

Por Kanter-Smoler, Gunilla, Fritzell, Kaisa, Rohlin, Anna, Engwall, Yvonne, Hallberg, Birgitta, Bergman, Annika, Meuller, Johan, Grönberg, Henrik, Karlsson, Per, Björk, Jan, Nordling, Margareta
Publicado em 2008

GREM 1 and POLE variants in hereditary colorectal cancer syndromes

Por Rohlin, Anna, Eiengård, Frida, Lundstam, Ulf, Zagoras, Theofanis, Nilsson, Staffan, Edsjö, Anders, Pedersen, Jan, Svensson, Janhenry, Skullman, Stefan, Karlsson, B. Göran, Björk, Jan, Nordling, Margareta
Publicado no Genes Chromosomes Cancer (2015)

Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

Por Rohlin, Anna, Rambech, Eva, Kvist, Anders, Törngren, Therese, Eiengård, Frida, Lundstam, Ulf, Zagoras, Theofanis, Gebre-Medhin, Samuel, Borg, Åke, Björk, Jan, Nilbert, Mef, Nordling, Margareta
Publicado no Fam Cancer (2016)