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Stuart Schwartz

Showing results (21-30 of 73) with videos related to

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Fertility and Sterility|January 9, 2004
Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complexLuAnn Judis, Ernest R Chan, Stuart Schwartz, et al.
Pediatric Neurology|January 25, 2005
Maternal uniparental disomy chromosome 14: case report and literature reviewMarni J Falk, Christine A Curtis, Nancy E Bass, et al.
Human Reproduction (Oxford, England)|July 25, 2006
Synaptic defects at meiosis I and non-obstructive azoospermiaDaniel Topping, Petrice Brown, LuAnn Judis, et al.
Human Molecular Genetics|August 30, 2007
Optimal design of oligonucleotide microarrays for measurement of DNA copy-numberAndrew J Sharp, Andy Itsara, Ze Cheng, et al.
Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Molecular Cytogenetics|July 21, 2021
Clinical significance and mechanisms associated with segmental UPDPeter R Papenhausen, Carla A Kelly, Samuel Harris, et al.
American Journal of Medical Genetics. Part A|April 30, 2025
Mosaicism for Genome Wide Homozygosity Identified as an Incidental Finding in Two Apparently Healthy Pregnant WomenGloria T Haskell, S Hussain Askree, Laura Kline, et al.
International Journal of Clinical and Experimental Pathology|January 19, 2013
Double-hit mantle cell lymphoma with MYC gene rearrangement or amplification: a report of four cases and review of the literatureReza Setoodeh, Stuart Schwartz, Peter Papenhausen, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosomeLeslie D Kulikowski, Laurie A Christ, Sintia I Nogueira, et al.
Molecular Cytogenetics|June 10, 2023
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarrayErica Soster, John Tynan, Clare Gibbons, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Fertility and Sterility|January 9, 2004
Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complexLuAnn Judis, Ernest R Chan, Stuart Schwartz, et al.
Pediatric Neurology|January 25, 2005
Maternal uniparental disomy chromosome 14: case report and literature reviewMarni J Falk, Christine A Curtis, Nancy E Bass, et al.
Human Reproduction (Oxford, England)|July 25, 2006
Synaptic defects at meiosis I and non-obstructive azoospermiaDaniel Topping, Petrice Brown, LuAnn Judis, et al.
Human Molecular Genetics|August 30, 2007
Optimal design of oligonucleotide microarrays for measurement of DNA copy-numberAndrew J Sharp, Andy Itsara, Ze Cheng, et al.
Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Molecular Cytogenetics|July 21, 2021
Clinical significance and mechanisms associated with segmental UPDPeter R Papenhausen, Carla A Kelly, Samuel Harris, et al.
American Journal of Medical Genetics. Part A|April 30, 2025
Mosaicism for Genome Wide Homozygosity Identified as an Incidental Finding in Two Apparently Healthy Pregnant WomenGloria T Haskell, S Hussain Askree, Laura Kline, et al.
International Journal of Clinical and Experimental Pathology|January 19, 2013
Double-hit mantle cell lymphoma with MYC gene rearrangement or amplification: a report of four cases and review of the literatureReza Setoodeh, Stuart Schwartz, Peter Papenhausen, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosomeLeslie D Kulikowski, Laurie A Christ, Sintia I Nogueira, et al.
Molecular Cytogenetics|June 10, 2023
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarrayErica Soster, John Tynan, Clare Gibbons, et al.
Pageof 8