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1 Ergebnisse
1
De novo mutations in FBRSL1 cause a novel recognizable malf..:
Ufartes, Roser
;
Berger, Hanna
;
Till, Katharina
...
EXC 2067: Multiscale Bioimaging. , 2020
Link:
https://resolver.sub.uni-goettingen.de/purl?gro-2/7082
RT Journal T1
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftsubgoettingen:oai:publications.goettingen-research-online.de:2_70825&Exemplar=1&LAN=DE A1 Ufartes, Roser A1 Berger, Hanna A1 Till, Katharina A1 Salinas, Gabriela A1 Sturm, Marc A1 Altmüller, Janine A1 Nürnberg, Peter A1 Thiele, Holger A1 Funke, Rudolf A1 Apeshiotis, Neophytos A1 Langen, Hendrik A1 Wollnik, Bernd A1 Borchers, Annette A1 Pauli, Silke A1 Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany A1 Department of Biology, Molecular Embryology, Philipps-University Marburg, Marburg, Germany A1 NGS Integrative Genomics Core Unit, University Medical Center Göttingen, Göttingen, Germany A1 Institute of Medical Genetics and Applied Genomics, Tübingen, Germany A1 Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany A1 Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany A1 Department of Neuropediatrics, Sozialpädiatrisches Zentrum, Kassel, Germany A1 Praxis für Humangenetik, Brunswick, Germany A1 Department of Neuropediatrics, Sozialpädiatrisches Zentrum Hannover, Hannover, Germany A1 Cluster of Excellence "Multiscale Bioimaging: From Molecular Machines To Networks of Excitable Cells" (MBExC), University of Göttingen, Göttingen, Germany A1 DFG Research Training Group, Membrane Plasticity in Tissue Development and Remodeling, GRK 2213, Philipps-University Marburg, Marburg, Germany YR 2020 JF EXC 2067: Multiscale Bioimaging LK http://dx.doi.org/https://resolver.sub.uni-goettingen.de/purl?gro-2/70825 DO https://resolver.sub.uni-goettingen.de/purl?gro-2/70825 SF ELIB - SuUB Bremen
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