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Number of items: 3.

Journal Article

Bausch, Birke, Schiavi, Francesca, Ni, Ying, Welander, Jenny, Patocs, Attila, Ngeow, Joanne ORCID: 0000-0003-1558-3627, Wellner, Ulrich ORCID: 0000-0002-8632-166X, Malinoc, Angelica, Taschin, Elisa, Barbon, Giovanni, Lanza, Virginia, Soederkvist, Peter, Stenman, Adam ORCID: 0000-0003-3248-7629, Larsson, Catharina, Svahn, Fredrika, Chen, Jin-Lian, Marquard, Jessica, Fraenkel, Merav, Walter, Martin A., Peczkowska, Mariola, Prejbisz, Aleksander ORCID: 0000-0001-7085-0244, Jarzab, Barbara ORCID: 0000-0001-9811-9584, Hasse-Lazar, Kornelia ORCID: 0000-0002-6430-0980, Petersenn, Stephan, Moeller, Lars C., Meyer, Almuth, Reisch, Nicole, Trupka, Arnold, Brase, Christoph, Galiano, Matthias, Preuss, Simon F., Kwok, Pingling, Lendvai, Nikoletta, Berisha, Gani, Makay, Ozer, Boedeker, Carsten C., Weryha, Georges, Racz, Karoly, Januszewicz, Andrzej, Walz, Martin K., Gimm, Oliver, Opocher, Giuseppe ORCID: 0000-0002-9845-9623, Eng, Charis and Neumann, Hartmut P. H. (2017). Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention. JAMA Oncol., 3 (9). S. 1204 - 1213. CHICAGO: AMER MEDICAL ASSOC. ISSN 2374-2445

Sullivan, Maren, Rybicki, Lisa A., Winter, Aurelia, Hoffmann, Michael M., Reiermann, Stefanie, Linke, Hannah, Arbeiter, Klaus, Patzer, Ludwig, Budde, Klemens ORCID: 0000-0002-7929-5942, Hoppe, Bernd, Zeier, Martin, Lhotta, Karl, Bock, Andreas, Wiech, Thorsten ORCID: 0000-0003-4053-1474, Gaspert, Ariana, Fehr, Thomas, Woznowski, Magdalena, Berisha, Gani, Malinoc, Angelica, Goek, Oemer-Necmi, Eng, Charis ORCID: 0000-0002-3693-5145 and Neumann, Hartmut P. H. (2011). Age-Related Penetrance of Hereditary Atypical Hemolytic Uremic Syndrome. Ann. Hum. Genet., 75. S. 639 - 648. HOBOKEN: WILEY. ISSN 1469-1809

Yehia, Lamis ORCID: 0000-0002-6389-3059, Seyfi, Marilyn, Niestroj, Lisa-Marie, Padmanabhan, Roshan, Ni, Ying, Frazier, Thomas W., Lal, Dennis and Eng, Charis (2020). Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations. JAMA Netw. Open, 3 (1). CHICAGO: AMER MEDICAL ASSOC. ISSN 2574-3805

This list was generated on Mon May 23 01:44:29 2022 CEST.