Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Bos DK"'
Autor:
Dijkstra AM; Section of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands., Evers-van Vliet K; Section of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands., Heiner-Fokkema MR; Laboratory of Metabolic Diseases, Department of Laboratory Medicine, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands., Bodewes FAJA; Section of Pediatric Gastroeneterology and Hepatology, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands., Bos DK; Department of Genetics, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands., Zsiros J; Princess Máxima Center for Pediatric Oncology, 3584 CX Utrecht, The Netherlands., van Aerde KJ; Department of Pediatric Infectious Disease and Immunology, Amalia's Children Hospital, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands., Koop K; Section Metabolic Diseases, Department of Pediatrics, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands., van Spronsen FJ; Section of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands., Lubout CMA; Section of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, The Netherlands.
Publikováno v:
International journal of neonatal screening [Int J Neonatal Screen] 2023 Dec 04; Vol. 9 (4). Date of Electronic Publication: 2023 Dec 04.
Autor:
Roht L; Department of Clinical Genetics, Genetic and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia.; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia., Hyldebrandt HK; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway., Stormorken AT; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway., Nordgarden H; Norwegian National Resource Centre for Oral Health in Rare Diagnosis, Lovisenberg Diaconal Hospital, Oslo, Norway., Sijmons RH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Bos DK; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Riegert-Johnson D; Department of Clinical Genetics and Genomics, Mayo Clinic, Jacksonville, Florida, USA., Mantia-Macklin S; Department of Clinical Genetics and Genomics, Mayo Clinic, Jacksonville, Florida, USA., Ilves P; Department of Radiology, Tartu University Hospital, Tartu, Estonia., Muru K; Department of Clinical Genetics, Genetic and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia.; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia., Wojcik MH; Broad Institute of MIT and Harvard, Massachusetts, Cambridge, USA.; Divisions of Genetics and Genomics and Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA., Kahre T; Department of Clinical Genetics, Genetic and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia.; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia., Õunap K; Department of Clinical Genetics, Genetic and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia.; Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
Publikováno v:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Jun; Vol. 11 (6), pp. e2157. Date of Electronic Publication: 2023 Mar 01.
Autor:
Imafidon ME; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Sikkema-Raddatz B; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Abbott KM; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Meems-Veldhuis MT; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Swertz MA; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.; Genomics Coordination Center, University of Groningen, University Medical Center Groningen, Groningen, Netherlands., van der Velde KJ; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.; Genomics Coordination Center, University of Groningen, University Medical Center Groningen, Groningen, Netherlands., Beunders G; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Bos DK; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Knoers NVAM; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., Kerstjens-Frederikse WS; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands., van Diemen CC; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Publikováno v:
Frontiers in pediatrics [Front Pediatr] 2021 May 31; Vol. 9, pp. 600556. Date of Electronic Publication: 2021 May 31 (Print Publication: 2021).
Autor:
Liisa Steinby, Aino Mäkikalli
This collection of essays studies the encounter between allegedly ahistorical concepts of narrative and eighteenth-century literature from across Europe. At issue is the question of whether the theoretical concepts underpinning narratology are, despi