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Caroline Schluth-Bolard

Showing results (1-10 of 71) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Structural and Mechanistic Diversity of Constitutional ChromoanagenesisSolène Doppler, Nicolas Chatron, Caroline Schluth-Bolard
Orphanet Journal of Rare Diseases|February 24, 2009
Distal Xq duplication and functional Xq disomyDamien Sanlaville, Caroline Schluth-Bolard, Catherine Turleau
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
ISCN and ChromoanagenesisMartine Doco-Fenzy, Jean-Michel Dupont, Caroline Schluth-Bolard
Nucleus (Austin, Tex.)|February 18, 2011
D4Z4 as a prototype of CTCF and lamins-dependent insulator in human cellsAlexandre Ottaviani, Caroline Schluth-Bolard, Eric Gilson, et al.
Psychiatric Genetics|September 14, 2023
Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skillsMarie-Noëlle Babinet, Nadine Thomas, Linda Pons, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
17p13.1 microdeletion involving the TP53 gene in a boy presenting with mental retardation but no tumorCaroline Schluth-Bolard, Damien Sanlaville, Audrey Labalme, et al.
Cytogenetic and Genome Research|April 5, 2019
Molecular Characterization of a Familial 13.6-Mb 20p11.1p12.1 Duplication without Clinical ConsequenceJulie Masson, Massimiliano Rossi, Audrey Labalme, et al.
Cytogenetic and Genome Research|December 22, 2017
Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric SequencesLyvia Marlet, Eudeline Alix, Marianne Till, et al.
American Journal of Medical Genetics. Part A|December 14, 2011
An 800  kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17pNadia Boutry-Kryza, Audrey Labalme, Marianne Till, et al.
BMC Medical Genetics|February 1, 2017
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literatureCaroline Demily, Alice Poisson, Elodie Peyroux, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Structural and Mechanistic Diversity of Constitutional ChromoanagenesisSolène Doppler, Nicolas Chatron, Caroline Schluth-Bolard
Orphanet Journal of Rare Diseases|February 24, 2009
Distal Xq duplication and functional Xq disomyDamien Sanlaville, Caroline Schluth-Bolard, Catherine Turleau
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
ISCN and ChromoanagenesisMartine Doco-Fenzy, Jean-Michel Dupont, Caroline Schluth-Bolard
Nucleus (Austin, Tex.)|February 18, 2011
D4Z4 as a prototype of CTCF and lamins-dependent insulator in human cellsAlexandre Ottaviani, Caroline Schluth-Bolard, Eric Gilson, et al.
Psychiatric Genetics|September 14, 2023
Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skillsMarie-Noëlle Babinet, Nadine Thomas, Linda Pons, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
17p13.1 microdeletion involving the TP53 gene in a boy presenting with mental retardation but no tumorCaroline Schluth-Bolard, Damien Sanlaville, Audrey Labalme, et al.
Cytogenetic and Genome Research|April 5, 2019
Molecular Characterization of a Familial 13.6-Mb 20p11.1p12.1 Duplication without Clinical ConsequenceJulie Masson, Massimiliano Rossi, Audrey Labalme, et al.
Cytogenetic and Genome Research|December 22, 2017
Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric SequencesLyvia Marlet, Eudeline Alix, Marianne Till, et al.
American Journal of Medical Genetics. Part A|December 14, 2011
An 800  kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17pNadia Boutry-Kryza, Audrey Labalme, Marianne Till, et al.
BMC Medical Genetics|February 1, 2017
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literatureCaroline Demily, Alice Poisson, Elodie Peyroux, et al.
Pageof 8