Nuchal cystic hygroma in five fetuses from 1819 to 1826 in the Meckel‐anatomical collections at the University of Halle, GermanyHow to cite this article: Göbbel L, Schultka R, Klunker R, Stock K, Helm J, Olsson L, Opitz JM, Gerlach A, Tönnies H. 2007. Nuchal cystic hygroma in five fetuses from 1819 to 1826 in the Meckel‐anatomical collections at the University of Halle, Germany. Am J Med Genet Part A 143A:119–128.

Autor: Göbbel, Luminita, Schultka, Rüdiger, Klunker, Rudyard, Stock, Karsten, Helm, Jürgen, Olsson, Lennart, Opitz, John M., Gerlach, Antje, Tönnies, Holger

Publikováno v: American Journal of Medical Genetics. Part A; January 2007, Vol. 143 Issue: 2 p119-128, 10p

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Towards interoperability in infection control: a standard data model for microbiology.

Autor: Rinaldi E; Berlin Institute of Health, Charité Universitätsmedizin, Berlin, Germany. eugenia.rinaldi@bih-charite.de., Drenkhahn C; Institute of Medical Informatics (IMI), University of Lübeck, Lübeck, Germany., Gebel B; Klinik für Infektiologie und Mikrobiologie, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Germany., Saleh K; Data Integration Center, Jena University Hospital, Jena, Germany., Tönnies H; Universitätsklinikum Münster, Münster, Germany., von Loewenich FD; Institute of Virology, University of Mainz, Mainz, Germany., Thoma N; Institute for Hygiene and Environmental Medicine, Charité Universitätsmedizin, Berlin, Germany., Baier C; Hannover Medical School, Institute for Medical Microbiology and Hospital Epidemiology, Hannover, Germany., Boeker M; Technische Universität München, München, Germany., Hinske LC; Institute for Digital Medicine, University Hospital Augsburg, Augsburg, Germany., Diaz LAP; Institute for Hygiene and Environmental Medicine, Charité Universitätsmedizin, Berlin, Germany., Behnke M; Institute for Hygiene and Environmental Medicine, Charité Universitätsmedizin, Berlin, Germany., Ingenerf J; Institute of Medical Informatics (IMI), University of Lübeck, Lübeck, Germany., Thun S; Berlin Institute of Health, Charité Universitätsmedizin, Berlin, Germany.

Publikováno v: Scientific data [Sci Data] 2023 Sep 23; Vol. 10 (1), pp. 654. Date of Electronic Publication: 2023 Sep 23.

Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study.

Autor: Rosenbohm A; Department of Neurology, University of Ulm, Ulm, Germany., Pott H; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Thomsen M; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Rafehi H; Division of Population Health and Immunity, The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.; Department of Medical Biology, The University of Melbourne, Parkville, Australia., Kaya S; Institute of Human Genetics, University Hospital Essen, Essen, Germany., Szymczak S; Insitute of Medical Biometry and Statistics, University of Lübeck, Lübeck, Germany., Volk AE; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Mueller K; Department of Neurology, University of Ulm, Ulm, Germany., Silveira I; i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal., Weishaupt JH; Division of Neurodegeneration, Neurology Department, University Medicine Mannheim, Heidelberg University, Mannheim, Germany., Tönnies H; Institute of Human Genetics, Christian-Albrechts-University, Kiel, Germany., Seibler P; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Zschiedrich K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Schaake S; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Westenberger A; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Zühlke C; Institute for Human Genetics, University of Lübeck, Lübeck, Germany., Depienne C; Institute of Human Genetics, University Hospital Essen, Essen, Germany., Trinh J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Ludolph AC; Department of Neurology, University of Ulm, Ulm, Germany.; German Center for Neurodegenerative Diseases, Site Ulm, Ulm, Germany., Klein C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Bahlo M; Division of Population Health and Immunity, The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.; Department of Medical Biology, The University of Melbourne, Parkville, Australia., Lohmann K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.

Publikováno v: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2022 Dec; Vol. 37 (12), pp. 2427-2439. Date of Electronic Publication: 2022 Sep 23.

Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease.

Autor: Stumm, M., Tönnies, H., Wieacker, P. F., Tönnies, H (AUTHOR)

Publikováno v: European Journal of Pediatrics. 1999, Vol. 158 Issue 7, p531-536. 6p.