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Koen Devriendt

Showing results (81-90 of 183) with videos related to

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American Journal of Medical Genetics. Part A|October 23, 2018
Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relativesJasmien Roosenboom, Robert Hermans, Frederik Lammens, et al.
Human Genetics|January 25, 2003
Duplication of the MID1 first exon in a patient with Opitz G/BBB syndromeJennifer Winter, Tanja Lehmann, Vanessa Suckow, et al.
Genome Medicine|September 28, 2012
Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human diseaseAlejandro Sifrim, Jeroen Kj Van Houdt, Leon-Charles Tranchevent, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 3, 2010
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER systemBenedetta Izzi, Brigitte Decallonne, Koen Devriendt, et al.
European Journal of Human Genetics : EJHG|June 21, 2007
Partial duplications of the ATRX gene cause the ATR-X syndromeBernard Thienpont, Thomy de Ravel, Hilde Van Esch, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 16, 2014
Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tractAnke Raaijmakers, Anniek Corveleyn, Koen Devriendt, et al.
Human Reproduction (Oxford, England)|February 4, 2017
Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryosEftychia Dimitriadou, Cindy Melotte, Sophie Debrock, et al.
The Journal of Pediatrics|May 17, 2011
Practical guidelines for managing patients with 22q11.2 deletion syndromeAnne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, et al.
European Journal of Human Genetics : EJHG|April 17, 2008
Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autismDries Castermans, Bernard Thienpont, Karolien Volders, et al.
European Journal of Human Genetics : EJHG|July 28, 2011
Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndromePeter Hammond, Femke Hannes, Michael Suttie, et al.
Pageof 19

Showing results (81-90 of 183) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics. Part A|October 23, 2018
Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relativesJasmien Roosenboom, Robert Hermans, Frederik Lammens, et al.
Human Genetics|January 25, 2003
Duplication of the MID1 first exon in a patient with Opitz G/BBB syndromeJennifer Winter, Tanja Lehmann, Vanessa Suckow, et al.
Genome Medicine|September 28, 2012
Annotate-it: a Swiss-knife approach to annotation, analysis and interpretation of single nucleotide variation in human diseaseAlejandro Sifrim, Jeroen Kj Van Houdt, Leon-Charles Tranchevent, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 3, 2010
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER systemBenedetta Izzi, Brigitte Decallonne, Koen Devriendt, et al.
European Journal of Human Genetics : EJHG|June 21, 2007
Partial duplications of the ATRX gene cause the ATR-X syndromeBernard Thienpont, Thomy de Ravel, Hilde Van Esch, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 16, 2014
Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tractAnke Raaijmakers, Anniek Corveleyn, Koen Devriendt, et al.
Human Reproduction (Oxford, England)|February 4, 2017
Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryosEftychia Dimitriadou, Cindy Melotte, Sophie Debrock, et al.
The Journal of Pediatrics|May 17, 2011
Practical guidelines for managing patients with 22q11.2 deletion syndromeAnne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, et al.
European Journal of Human Genetics : EJHG|April 17, 2008
Position effect leading to haploinsufficiency in a mosaic ring chromosome 14 in a boy with autismDries Castermans, Bernard Thienpont, Karolien Volders, et al.
European Journal of Human Genetics : EJHG|July 28, 2011
Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndromePeter Hammond, Femke Hannes, Michael Suttie, et al.
Pageof 19