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Alexandre Reymond

Showing results (41-50 of 169) with videos related to

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European Journal of Medical Genetics|January 17, 2017
Inflammatory myopathy in a patient with Aicardi-Goutières syndromeBirutė Tumienė, Norine Voisin, Eglė Preikšaitienė, et al.
Gene|November 5, 2003
Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12Marc Friedli, Michel Guipponi, Sonia Bertrand, et al.
Genome Research|December 14, 2005
Tandem chimerism as a means to increase protein complexity in the human genomeGenís Parra, Alexandre Reymond, Noura Dabbouseh, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligaseLucia Micale, Carmela Fusco, Bartolomeo Augello, et al.
American Journal of Human Genetics|July 11, 2006
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesGiuseppe Merla, Cédric Howald, Charlotte N Henrichsen, et al.
Nature Genetics|March 10, 2009
Segmental copy number variation shapes tissue transcriptomesCharlotte N Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.
Molecular Psychiatry|June 29, 2022
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndromeMaris Alver, Valentina Mancini, Kristi Läll, et al.
Human Molecular Genetics|May 13, 2008
Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndromeJessica Molina, Paulina Carmona-Mora, Jacqueline Chrast, et al.
Genome Medicine|January 7, 2024
Rare copy-number variants as modulators of common disease susceptibilityChiara Auwerx, Maarja Jõeloo, Marie C Sadler, et al.
Journal of Pediatric Genetics|May 13, 2017
A New Split Hand/Foot Malformation with Long Bone Deficiency Familial CaseCarmela Fusco, Pasquelena De Nittis, Ali Abdullah Alfaiz, et al.
Pageof 17

Showing results (41-50 of 169) with videos related to

Sort By:
Pageof 17
European Journal of Medical Genetics|January 17, 2017
Inflammatory myopathy in a patient with Aicardi-Goutières syndromeBirutė Tumienė, Norine Voisin, Eglė Preikšaitienė, et al.
Gene|November 5, 2003
Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12Marc Friedli, Michel Guipponi, Sonia Bertrand, et al.
Genome Research|December 14, 2005
Tandem chimerism as a means to increase protein complexity in the human genomeGenís Parra, Alexandre Reymond, Noura Dabbouseh, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligaseLucia Micale, Carmela Fusco, Bartolomeo Augello, et al.
American Journal of Human Genetics|July 11, 2006
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesGiuseppe Merla, Cédric Howald, Charlotte N Henrichsen, et al.
Nature Genetics|March 10, 2009
Segmental copy number variation shapes tissue transcriptomesCharlotte N Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.
Molecular Psychiatry|June 29, 2022
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndromeMaris Alver, Valentina Mancini, Kristi Läll, et al.
Human Molecular Genetics|May 13, 2008
Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndromeJessica Molina, Paulina Carmona-Mora, Jacqueline Chrast, et al.
Genome Medicine|January 7, 2024
Rare copy-number variants as modulators of common disease susceptibilityChiara Auwerx, Maarja Jõeloo, Marie C Sadler, et al.
Journal of Pediatric Genetics|May 13, 2017
A New Split Hand/Foot Malformation with Long Bone Deficiency Familial CaseCarmela Fusco, Pasquelena De Nittis, Ali Abdullah Alfaiz, et al.
Pageof 17