Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Publikationen

Suchbegriffe: FMR1, . Treffer: 6

2013

Rinner, B; Weinhaeusel, A; Lohberger, B; Froehlich, EV; Pulverer, W; Fischer, C; Meditz, K; Scheipl, S; Trajanoski, S; Guelly, C; Leithner, A; Liegl, B Chordoma characterization of significant changes of the DNA methylation pattern.
PLoS One. 2013; 8(3):e56609-e56609 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Tea, MK; Weghofer, A; Wagner, K; Singer, CF Association of BRCA1/2 mutations with FMR1 genotypes: effects on menarcheal and menopausal age.
Maturitas. 2013; 75(2):148-151
Web of Science PubMed FullText FullText_MUG

 

2012

Borbas, P; Leithner, A; Sadoghi, P; Berndt, A; Liegl, B; Haas, OA Clonality assessment in a case of multifocal adamantinoma and a review of the literature.
Case Rep Med. 2012; 2012(1):605685-605685 [OPEN ACCESS]
PubMed PUBMED Central FullText FullText_MUG

 

Weghofer, A; Tea, MK; Barad, DH; Kim, A; Singer, CF; Wagner, K; Gleicher, N BRCA1/2 mutations appear embryo-lethal unless rescued by low (CGG n<26) FMR1 sub-genotypes: explanation for the "BRCA paradox"?
PLoS One. 2012; 7(9):e44753-e44753 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

2005

Leithner, A; Weinhaeusel, A; Zeitlhofer, P; Koch, H; Radl, R; Windhager, R; Beham, A; Haas, OA Evidence of a polyclonal nature of myositis ossificans.
Virchows Arch. 2005; 446(4):438-441
Web of Science PubMed FullText FullText_MUG

 

1999

Petek, E; Kroisel, PM; Schuster, M; Zierler, H; Wagner, K Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene.
Am J Med Genet. 1999; 84(3):229-232 (- Case Report)
Web of Science PubMed FullText

 

© Meduni Graz Impressum