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Björn Menten

Showing results (1-10 of 151) with videos related to

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Molecular Vision|February 13, 2013
Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndromeSarah Vergult, Bart Leroy, Ilse Claerhout, et al.
Human Reproduction Update|March 7, 2020
Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemmaMina Popovic, Lien Dhaenens, Annekatrien Boel, et al.
Human Reproduction Update|April 17, 2020
Erratum. Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemmaMina Popovic, Lien Dhaenens, Annekatrien Boel, et al.
Nucleic Acids Research|December 20, 2018
WisecondorX: improved copy number detection for routine shallow whole-genome sequencingLennart Raman, Annelies Dheedene, Matthias De Smet, et al.
Biomolecular Detection and Quantification|August 24, 2016
Flexible analysis of digital PCR experiments using generalized linear mixed modelsMatthijs Vynck, Jo Vandesompele, Nele Nijs, et al.
Genes|April 23, 2022
Expanding the Phenotype of B3GALNT2-Related DisordersErika D'haenens, Sarah Vergult, Björn Menten, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndromeKaren Buysse, Björn Menten, Ann Oostra, et al.
European Journal of Pediatrics|August 12, 2011
4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndromeGoran Cuturilo, Björn Menten, Aleksandar Krstic, et al.
Prenatal Diagnosis|June 21, 2019
PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction predictionLennart Raman, Machteld Baetens, Matthias De Smet, et al.
BMC Medical Genetics|September 16, 2009
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samplesBjörn Menten, Katrien Swerts, Barbara Delle Chiaie, et al.
Pageof 16

Showing results (1-10 of 151) with videos related to

Sort By:
Pageof 16
Molecular Vision|February 13, 2013
Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndromeSarah Vergult, Bart Leroy, Ilse Claerhout, et al.
Human Reproduction Update|March 7, 2020
Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemmaMina Popovic, Lien Dhaenens, Annekatrien Boel, et al.
Human Reproduction Update|April 17, 2020
Erratum. Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemmaMina Popovic, Lien Dhaenens, Annekatrien Boel, et al.
Nucleic Acids Research|December 20, 2018
WisecondorX: improved copy number detection for routine shallow whole-genome sequencingLennart Raman, Annelies Dheedene, Matthias De Smet, et al.
Biomolecular Detection and Quantification|August 24, 2016
Flexible analysis of digital PCR experiments using generalized linear mixed modelsMatthijs Vynck, Jo Vandesompele, Nele Nijs, et al.
Genes|April 23, 2022
Expanding the Phenotype of B3GALNT2-Related DisordersErika D'haenens, Sarah Vergult, Björn Menten, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndromeKaren Buysse, Björn Menten, Ann Oostra, et al.
European Journal of Pediatrics|August 12, 2011
4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndromeGoran Cuturilo, Björn Menten, Aleksandar Krstic, et al.
Prenatal Diagnosis|June 21, 2019
PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction predictionLennart Raman, Machteld Baetens, Matthias De Smet, et al.
BMC Medical Genetics|September 16, 2009
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samplesBjörn Menten, Katrien Swerts, Barbara Delle Chiaie, et al.
Pageof 16