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Jasmin Beygo

Showing results (11-20 of 45) with videos related to

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Journal of Molecular Medicine (Berlin, Germany)|March 25, 2014
Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testingThomas Eggermann, Ann-Kathrin Heilsberg, Susanne Bens, et al.
Human Molecular Genetics|October 23, 2014
Epigenetic germline mosaicism in infertile menSandra Laurentino, Jasmin Beygo, Verena Nordhoff, et al.
European Journal of Human Genetics : EJHG|April 11, 2013
Evidence for anticipation in Beckwith-Wiedemann syndromeSiren Berland, Mia Appelbäck, Ove Bruland, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literatureAnna Le Fevre, Jasmin Beygo, Cheryl Silveira, et al.
Plos One|October 17, 2013
Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defectsJasmin Beygo, Ole Ammerpohl, Daniela Gritzan, et al.
European Journal of Human Genetics : EJHG|February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndromeJasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Genes|March 29, 2023
<i>FGF9</i>-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational FamilyAriane Schmetz, Jörg Schaper, Simon Thelen, et al.
Pediatric Blood & Cancer|April 2, 2026
MYCN Amplification in RB1-Inactivated Retinoblastoma: Association With High-Risk FeaturesKyriaki Papaioannou, Regina Kubica, Karen Fischhuber, et al.
Molecular Genetics & Genomic Medicine|November 28, 2017
The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Thomas Eggermann, Barbara Oehl-Jaschkowitz, Severin Dicks, et al.
Epigenetics|December 3, 2016
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domainsDavid Monk, Joannella Morales, Johan T den Dunnen, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Journal of Molecular Medicine (Berlin, Germany)|March 25, 2014
Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testingThomas Eggermann, Ann-Kathrin Heilsberg, Susanne Bens, et al.
Human Molecular Genetics|October 23, 2014
Epigenetic germline mosaicism in infertile menSandra Laurentino, Jasmin Beygo, Verena Nordhoff, et al.
European Journal of Human Genetics : EJHG|April 11, 2013
Evidence for anticipation in Beckwith-Wiedemann syndromeSiren Berland, Mia Appelbäck, Ove Bruland, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literatureAnna Le Fevre, Jasmin Beygo, Cheryl Silveira, et al.
Plos One|October 17, 2013
Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defectsJasmin Beygo, Ole Ammerpohl, Daniela Gritzan, et al.
European Journal of Human Genetics : EJHG|February 4, 2016
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndromeJasmin Beygo, Ivana Joksic, Tim M Strom, et al.
Genes|March 29, 2023
<i>FGF9</i>-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational FamilyAriane Schmetz, Jörg Schaper, Simon Thelen, et al.
Pediatric Blood & Cancer|April 2, 2026
MYCN Amplification in RB1-Inactivated Retinoblastoma: Association With High-Risk FeaturesKyriaki Papaioannou, Regina Kubica, Karen Fischhuber, et al.
Molecular Genetics & Genomic Medicine|November 28, 2017
The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?Thomas Eggermann, Barbara Oehl-Jaschkowitz, Severin Dicks, et al.
Epigenetics|December 3, 2016
Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domainsDavid Monk, Joannella Morales, Johan T den Dunnen, et al.
Pageof 5