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Lisanne Vervoort

Showing results (1-10 of 6) with videos related to

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Genes|November 24, 2022
The 22q11.2 Low Copy RepeatsLisanne Vervoort, Joris Robert Vermeesch
Frontiers in Genetics|August 2, 2021
22q11.2 Low Copy Repeats Expanded in the Human LineageLisanne Vervoort, Nicolas Dierckxsens, Zjef Pereboom, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
Human Molecular Genetics|December 30, 2019
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic originsLisanne Vervoort, Wolfram Demaerel, Laura Y Rengifo, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Genes|November 24, 2022
The 22q11.2 Low Copy RepeatsLisanne Vervoort, Joris Robert Vermeesch
Frontiers in Genetics|August 2, 2021
22q11.2 Low Copy Repeats Expanded in the Human LineageLisanne Vervoort, Nicolas Dierckxsens, Zjef Pereboom, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion SyndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|November 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndromeLisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
Human Molecular Genetics|December 30, 2019
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic originsLisanne Vervoort, Wolfram Demaerel, Laura Y Rengifo, et al.
Pageof 1