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Gert Matthijs

Showing results (41-50 of 199) with videos related to

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European Journal of Medical Genetics|December 2, 2008
Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutationHilde Van Esch, Luc Buekenhout, Valerie Race, et al.
Biochimica Et Biophysica Acta|September 22, 2009
CDG nomenclature: time for a change!Jaak Jaeken, Thierry Hennet, Gert Matthijs, et al.
Bulletin of the World Health Organization|May 20, 2006
A clearing house for diagnostic testing: the solution to ensure access to and use of patented genetic inventions?Esther van Zimmeren, Birgit Verbeure, Gert Matthijs, et al.
Current Molecular Medicine|September 11, 2008
Multi-system disorder syndromes associated with cystinuria type IKevin Martens, Jaak Jaeken, Gert Matthijs, et al.
Nature Biotechnology|August 10, 2013
The European BRCA patent oppositions and appeals: coloring inside the linesGert Matthijs, Isabelle Huys, Geertrui Van Overwalle, et al.
American Journal of Medical Genetics. Part A|July 13, 2012
DPAGT1-CDG: report of a patient with fetal hypokinesia phenotypeIgnacio Arroyo Carrera, Gert Matthijs, Belen Perez, et al.
Nature Reviews. Genetics|December 31, 2005
Models for facilitating access to patents on genetic inventionsGeertrui Van Overwalle, Esther van Zimmeren, Birgit Verbeure, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
Variability in the use of CE-marked assays for in vitro diagnostics of CFTR gene mutations in European genetic testing laboratoriesJana Camajova, Sarah Berwouts, Gert Matthijs, et al.
Trends in Biotechnology|January 31, 2006
Patent pools and diagnostic testingBirgit Verbeure, Esther van Zimmeren, Gert Matthijs, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutation in a large family with Noonan syndrome and dizygous twinningEls Schollen, Gert Matthijs, Marc Gewillig, et al.
Pageof 20

Showing results (41-50 of 199) with videos related to

Sort By:
Pageof 20
European Journal of Medical Genetics|December 2, 2008
Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutationHilde Van Esch, Luc Buekenhout, Valerie Race, et al.
Biochimica Et Biophysica Acta|September 22, 2009
CDG nomenclature: time for a change!Jaak Jaeken, Thierry Hennet, Gert Matthijs, et al.
Bulletin of the World Health Organization|May 20, 2006
A clearing house for diagnostic testing: the solution to ensure access to and use of patented genetic inventions?Esther van Zimmeren, Birgit Verbeure, Gert Matthijs, et al.
Current Molecular Medicine|September 11, 2008
Multi-system disorder syndromes associated with cystinuria type IKevin Martens, Jaak Jaeken, Gert Matthijs, et al.
Nature Biotechnology|August 10, 2013
The European BRCA patent oppositions and appeals: coloring inside the linesGert Matthijs, Isabelle Huys, Geertrui Van Overwalle, et al.
American Journal of Medical Genetics. Part A|July 13, 2012
DPAGT1-CDG: report of a patient with fetal hypokinesia phenotypeIgnacio Arroyo Carrera, Gert Matthijs, Belen Perez, et al.
Nature Reviews. Genetics|December 31, 2005
Models for facilitating access to patents on genetic inventionsGeertrui Van Overwalle, Esther van Zimmeren, Birgit Verbeure, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
Variability in the use of CE-marked assays for in vitro diagnostics of CFTR gene mutations in European genetic testing laboratoriesJana Camajova, Sarah Berwouts, Gert Matthijs, et al.
Trends in Biotechnology|January 31, 2006
Patent pools and diagnostic testingBirgit Verbeure, Esther van Zimmeren, Gert Matthijs, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutation in a large family with Noonan syndrome and dizygous twinningEls Schollen, Gert Matthijs, Marc Gewillig, et al.
Pageof 20