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Koen Devriendt

Showing results (1-10 of 183) with videos related to

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Human Reproduction Update|January 29, 2005
Hydatidiform mole and triploidy: the role of genomic imprinting in placental developmentKoen Devriendt
European Journal of Medical Genetics|February 8, 2006
Human laterality disordersHilde Peeters, Koen Devriendt
Human Genomics|December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalitiesKoen Devriendt, Joris R Vermeesch
European Journal of Pediatrics|August 4, 2004
Diagnostic evaluation for asymmetry: consider genetic mosaicismKoen Devriendt, Jean-Pierre Fryns
Clinical Dysmorphology|June 9, 2006
Anterior cervical hypertrichosis and mental retardationBernard Thienpont, Joris Vermeesch, Koen Devriendt
European Journal of Human Genetics : EJHG|February 4, 2010
Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)Eberhard Schwinger, Koen Devriendt, Anita Rauch, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality: a new constellation or deletion in chromosome 22q11.2?Koen Devriendt, Ann Swillen, Ingeborg Stalmans, et al.
American Journal of Medical Genetics. Part A|September 24, 2004
Multiple circumferential skin creases: another sign of genetic mosaicism?Koen Devriendt, J P Fryns, C Vanhole, et al.
European Journal of Medical Genetics|September 17, 2016
Bilateral renal tumors in an adult man with Smith-Magenis syndrome: The role of the FLCN geneLeila Dardour, Pieter Verleyen, Karl Lesage, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 25, 2003
Triangular face and vascular malformation. The links to renal failureAnne Wauters, Tom Dejagere, Koen Devriendt, et al.
Pageof 19

Showing results (1-10 of 183) with videos related to

Sort By:
Pageof 19
Human Reproduction Update|January 29, 2005
Hydatidiform mole and triploidy: the role of genomic imprinting in placental developmentKoen Devriendt
European Journal of Medical Genetics|February 8, 2006
Human laterality disordersHilde Peeters, Koen Devriendt
Human Genomics|December 17, 2004
Chromosomal phenotypes and submicroscopic abnormalitiesKoen Devriendt, Joris R Vermeesch
European Journal of Pediatrics|August 4, 2004
Diagnostic evaluation for asymmetry: consider genetic mosaicismKoen Devriendt, Jean-Pierre Fryns
Clinical Dysmorphology|June 9, 2006
Anterior cervical hypertrichosis and mental retardationBernard Thienpont, Joris Vermeesch, Koen Devriendt
European Journal of Human Genetics : EJHG|February 4, 2010
Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)Eberhard Schwinger, Koen Devriendt, Anita Rauch, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality: a new constellation or deletion in chromosome 22q11.2?Koen Devriendt, Ann Swillen, Ingeborg Stalmans, et al.
American Journal of Medical Genetics. Part A|September 24, 2004
Multiple circumferential skin creases: another sign of genetic mosaicism?Koen Devriendt, J P Fryns, C Vanhole, et al.
European Journal of Medical Genetics|September 17, 2016
Bilateral renal tumors in an adult man with Smith-Magenis syndrome: The role of the FLCN geneLeila Dardour, Pieter Verleyen, Karl Lesage, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 25, 2003
Triangular face and vascular malformation. The links to renal failureAnne Wauters, Tom Dejagere, Koen Devriendt, et al.
Pageof 19