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Gert Matthijs

Showing results (11-20 of 199) with videos related to

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European Journal of Human Genetics : EJHG|June 18, 2008
Patenting and licensing in genetic testing: ethical, legal, and social issuesSirpa Soini, Ségolène Aymé, Gert Matthijs, et al.
European Journal of Human Genetics : EJHG|June 17, 2008
Patenting and licensing in genetic testing: recommendations of the European Society of Human GeneticsS Aymé, Gert Matthijs, S Soini, et al.
European Journal of Human Genetics : EJHG|August 6, 2015
Clinical utility gene card for: DPAGT1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|October 29, 2015
New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testingGert Matthijs, Anna Dierking, Jörg Schmidtke
European Journal of Human Genetics : EJHG|February 5, 2015
Clinical utility gene card for: ALG1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
Pediatric Research|November 1, 2002
Congenital disorders of glycosylation: a reviewStephanie Grunewald, Gert Matthijs, Jaak Jaeken
European Journal of Human Genetics : EJHG|February 27, 2014
Clinical utility gene card for: Phosphomannose isomerase deficiencyJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|July 24, 2014
Clinical utility gene card for: ALG6 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|January 16, 2014
Clinical utility gene card for: Phosphomannomutase 2 deficiencyJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|June 25, 2019
Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylationJaak Jaeken, Dirk J Lefeber, Gert Matthijs
Pageof 20

Showing results (11-20 of 199) with videos related to

Sort By:
Pageof 20
European Journal of Human Genetics : EJHG|June 18, 2008
Patenting and licensing in genetic testing: ethical, legal, and social issuesSirpa Soini, Ségolène Aymé, Gert Matthijs, et al.
European Journal of Human Genetics : EJHG|June 17, 2008
Patenting and licensing in genetic testing: recommendations of the European Society of Human GeneticsS Aymé, Gert Matthijs, S Soini, et al.
European Journal of Human Genetics : EJHG|August 6, 2015
Clinical utility gene card for: DPAGT1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|October 29, 2015
New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testingGert Matthijs, Anna Dierking, Jörg Schmidtke
European Journal of Human Genetics : EJHG|February 5, 2015
Clinical utility gene card for: ALG1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
Pediatric Research|November 1, 2002
Congenital disorders of glycosylation: a reviewStephanie Grunewald, Gert Matthijs, Jaak Jaeken
European Journal of Human Genetics : EJHG|February 27, 2014
Clinical utility gene card for: Phosphomannose isomerase deficiencyJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|July 24, 2014
Clinical utility gene card for: ALG6 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|January 16, 2014
Clinical utility gene card for: Phosphomannomutase 2 deficiencyJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|June 25, 2019
Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylationJaak Jaeken, Dirk J Lefeber, Gert Matthijs
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