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Bioethics|September 29, 2004
Pharmacogenetic testing, informed consent and the problem of secondary informationChristian Netzer, Nikola Biller-Andorno
Wiener Medizinische Wochenschrift (1946)|June 10, 2015
Osteogenesis imperfecta: pathophysiology and treatmentHeike Hoyer-Kuhn, Christian Netzer, Oliver Semler
Molecular and Cellular Probes|March 28, 2019
Which genes to assess in the NGS diagnostics of intellectual disability? The case for a consensus database-driven and expert-curated approachFlorian Erger, Christian P Schaaf, Christian Netzer
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Carrier testing for autosomal recessive disorders: a look at current practice in GermanyChristian Netzer, Clara Velmans, Florian Erger, et al.
European Journal of Medical Genetics|July 2, 2013
Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9pIris Bartels, Irene Pütz, Nadine Reintjes, et al.
Orphanet Journal of Rare Diseases|September 20, 2019
Individualized treatment with denosumab in children with osteogenesis imperfecta - follow up of a trial cohortHeike Hoyer-Kuhn, Mirko Rehberg, Christian Netzer, et al.
Orphanet Journal of Rare Diseases|September 27, 2014
Two years' experience with denosumab for children with osteogenesis imperfecta type VIHeike Hoyer-Kuhn, Christian Netzer, Friederike Koerber, et al.
Biochemical and Biophysical Research Communications|August 30, 2002
Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1Christian Netzer, Stefan K Bohlander, Leonie Rieger, et al.
Biochimica Et Biophysica Acta|January 31, 2006
Defining the heterochromatin localization and repression domains of SALL1Christian Netzer, Stefan K Bohlander, Markus Hinzke, et al.
European Journal of Human Genetics : EJHG|June 13, 2018
Uniparental isodisomy as a cause of recessive Mendelian disease: a diagnostic pitfall with a quick and easy solution in medium/large NGS analysesFlorian Erger, Karin Burau, Michael Elsässer, et al.
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