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Autor:
Olayiwola, Joie O.1,2 (AUTHOR), Marhabaie, Mohammad1 (AUTHOR), Koboldt, Daniel1,3 (AUTHOR), Matthews, Theodora1,3 (AUTHOR), Siemon, Amy1,3 (AUTHOR), Mouhlas, Danielle1,3 (AUTHOR), Porter, Taylor1,3 (AUTHOR), Kyle, George1,3 (AUTHOR), Myers, Cortlandt1,3 (AUTHOR), Mei, Hui1,2,3 (AUTHOR), Hou, Ying‐Chen Claire1,2,3 (AUTHOR), Babcock, Melanie1,2,3 (AUTHOR), Hunter, Jesse1,2,3 (AUTHOR), Schieffer, Kathleen M.1,2,3 (AUTHOR), Akkari, Yassmine1,2 (AUTHOR), Reshmi, Shalini1,2,3 (AUTHOR), Cottrell, Catherine1,2,3 (AUTHOR), Mathew, Mariam T.1,2,3 (AUTHOR), Leung, Marco L.1,2,3 (AUTHOR) marco.leung@nationwidechildrens.org
Publikováno v:
Molecular Genetics & Genomic Medicine. Mar2024, Vol. 12 Issue 3, p1-14. 14p.
Autor:
Hehir-Kwa JY; Department of Human Genetics, Radboud UMC, Nijmegen, The Netherlands.; Donders Centre of Cognitive Science, Nijmegen, The Netherlands., Claustres M; Department of Molecular Genetics, IURC (Institut Universitaire de Recherche Clinique), Montpellier, France., Hastings RJ; CEQAS, Women's Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, England., van Ravenswaaij-Arts C; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands., Christenhusz G; Centre for Biomedical Ethics and Law, University of Leuven, Leuven, Belgium., Genuardi M; Institute of Medical Genetics, 'A. Gemelli' School of Medicine, Catholic University of the Sacred Heart, Rome, Italy., Melegh B; Department of Medical Genetics, University of Pécs, Pécs, Hungary., Cambon-Thomsen A; Institut national de la santé et de la recherche médicale and Université Toulouse III-Paul Sabatier joint Unit 1027, Faculty of Medicine, Toulouse, France., Patsalis P; Translational Genetics Team, The Cyprus Institute of Neurology & Genetics, Cyprus School of Molecular Medicine, Nicosia, Cyprus., Vermeesch J; Centre for Human Genetics, University Hospital Leuven, Department of Human Genetics, KU Leuven, Leuven, Belgium., Cornel MC; Clinical Genetics & EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands., Searle B; Unique (Rare Chromosome Disorder Support Group), Oxted, England., Palotie A; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland., Capoluongo E; SIBioC Clinical Molecular Diagnostic Training School, Istituto di Biochimica Clinica, Università Cattolica del S. Cuore, Rome, Italy., Peterlin B; Department of Obstetrics and Gynecology, Clinical Institute of Medical Genetics, University Medical Centre Ljubljana, Ljubljana, Slovenia., Estivill X; Center for Genomic Regulation (CRG), Barcelona, Spain.; Pompeu Fabra University (UPF), Barcelona, Spain.; Dexeus Women's Health Quiron-Dexeus University Institute, Barcelona, Spain., Robinson PN; Institut für Medizinische Genetik und Humangenetik, Charité - Universitätsmedizin Berlin, Berlin, Germany.; Berlin Brandenburg Center for Regenerative Therapies, Charité - Universitätsmedizin Berlin, Berlin, Germany.; Department of Mathematics and Computer Science, Institute for Bioinformatics, Freie Universität Berlin, Berlin, Germany.
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Dec; Vol. 23 (12), pp. 1601-6. Date of Electronic Publication: 2015 Jun 03.
Autor:
Brady PD; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium., Delle Chiaie B; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Christenhusz G; Centre for Biomedical Ethics and Law, Faculty of Medicine, KU Leuven, Leuven, Belgium., Dierickx K; Centre for Biomedical Ethics and Law, Faculty of Medicine, KU Leuven, Leuven, Belgium., Van Den Bogaert K; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium., Menten B; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Janssens S; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Defoort P; Department of Obstetrics and Gynaecology, Ghent University Hospital, Ghent, Belgium., Roets E; Department of Obstetrics and Gynaecology, Ghent University Hospital, Ghent, Belgium., Sleurs E; Department of Obstetrics and Gynaecology, Ghent University Hospital, Ghent, Belgium., Keymolen K; Center for Medical Genetics, Universitair Ziekenhuis Brussels, Vrije Universiteit Brussels, Brussels, Belgium., De Catte L; 1] Department of Development and Regeneration, Unit Pregnancy, Foetus and Newborn, KU Leuven, Leuven, Belgium [2] Department of Obstetrics and Gynaecology, University Hospital Leuven, KU Leuven, Leuven, Belgium., Deprest J; 1] Department of Development and Regeneration, Unit Pregnancy, Foetus and Newborn, KU Leuven, Leuven, Belgium [2] Department of Obstetrics and Gynaecology, University Hospital Leuven, KU Leuven, Leuven, Belgium., de Ravel T; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium., Van Esch H; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium., Fryns JP; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium., Devriendt K; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium., Vermeesch JR; Centre for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium.
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2014 Jun; Vol. 16 (6), pp. 469-76. Date of Electronic Publication: 2013 Oct 31.
Publikováno v:
The American journal of bioethics : AJOB [Am J Bioeth] 2014; Vol. 14 (3), pp. 31-3.
Autor:
Oladayo, Abimbola M., Prochaska, Sydney, Busch, Tamara, Adeyemo, Wasiu L., Gowans, Lord J. J., Eshete, Mekonen, Awotoye, Waheed, Sule, Veronica, Alade, Azeez, Adeyemo, Adebowale A., Mossey, Peter A., Prince, Anya, Murray, Jeffrey C., Butali, Azeez
Publikováno v:
AJOB Empirical Bioethics; Apr-Jun2024, Vol. 15 Issue 2, p133-146, 14p
Autor:
Singh, Rajesh R.1 (AUTHOR) rajesh.r.singh@questdiagnostics.com
Publikováno v:
Diagnostics (2075-4418). Jul2022, Vol. 12 Issue 7, pN.PAG-N.PAG. 14p.
Autor:
Fischer, Julie1 (AUTHOR), Rohena, Luis2,3 (AUTHOR)
Publikováno v:
Case Reports in Genetics. 5/17/2022, p1-5. 5p.
Autor:
Cheung F; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada., Birch P; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada., Friedman JM; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada., Elliott AM; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.; BC Women's Health Research Institute, Vancouver, British Columbia, Canada., Adam S; Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Publikováno v:
Journal of genetic counseling [J Genet Couns] 2022 Aug; Vol. 31 (4), pp. 887-900. Date of Electronic Publication: 2022 Feb 06.
Autor:
Mastromoro, Gioia1 (AUTHOR) daniele.guadagnolo@uniroma1.it, Guadagnolo, Daniele1 (AUTHOR), Khaleghi Hashemian, Nader1 (AUTHOR), Marchionni, Enrica1 (AUTHOR), Traversa, Alice1 (AUTHOR), Pizzuti, Antonio1 (AUTHOR)
Publikováno v:
Diagnostics (2075-4418). Mar2022, Vol. 12 Issue 3, p575-575. 35p.