Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unb...

Tekijä Wieczorek, D, Engels, H, Viersbach, R, Henke, B, Schwanitz, G, Passarge, E
Julkaistu 1998

5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability

Tekijä Kleffmann, W., Zink, A.M., Lee, J.A., Senderek, J., Mangold, E., Moog, U., Rappold, G.A., Wohlleber, E., Engels, H.
Julkaistu 2012

Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability – Further Delineation of the Phenotype and Expression Studies

Tekijä Zink, A.M., Wohlleber, E., Engels, H., Rødningen, O.K., Ravn, K., Heilmann, S., Rehnitz, J., Katzorke, N., Kraus, C., Blichfeldt, S., Hoffmann, P., Reutter, H., Brockschmidt, F.F., Kreiß-Nachtsheim, M., Vogt, P.H., Prescott, T.E., Tümer, Z., Lee, J.A.
Julkaistu 2014

Risk of cancer after low doses of ionising radiation: retrospective cohort study in 15 countries

Tekijä Cardis, E, Vrijheid, M, Blettner, M, Gilbert, E, Hakama, M, Hill, C, Howe, G, Kaldor, J, Muirhead, C R, Schubauer-Berigan, M, Yoshimura, T, Bermann, F, Cowper, G, Fix, J, Hacker, C, Heinmiller, B, Marshall, M, Thierry-Chef, I, Utterback, D, Ahn, Y-O, Amoros, E, Ashmore, P, Auvinen, A, Bae, J-M, Solano, J Bernar, Biau, A, Combalot, E, Deboodt, P, Sacristan, A Diez, Eklof, M, Engels, H, Engholm, G, Gulis, G, Habib, R, Holan, K, Hyvonen, H, Kerekes, A, Kurtinaitis, J, Malker, H, Martuzzi, M, Mastauskas, A, Monnet, A, Moser, M, Pearce, M S, Richardson, D B, Rodriguez-Artalejo, F, Rogel, A, Tardy, H, Telle-Lamberton, M, Turai, I, Usel, M, Veress, K
Julkaistu 2005