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Stephanie L Sherman

Showing results (11-20 of 122) with videos related to

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Human Genetics|February 6, 2004
A study of the distributional characteristics of FMR1 transcript levels in 238 individualsEmily G Allen, Weiya He, Maneesha Yadav-Shah, et al.
G3 (Bethesda, Md.)|October 14, 2016
Genome-Wide Association Study of Meiotic Recombination PhenotypesFerdouse Begum, Reshmi Chowdhury, Vivian G Cheung, et al.
Genetic Epidemiology|January 30, 2004
A trisomic transmission disequilibrium testZhiying Xu, Kimberly F Kerstann, Stephanie L Sherman, et al.
American Journal of Human Genetics|November 20, 2004
Association between maternal age and meiotic recombination for trisomy 21Neil E Lamb, Kai Yu, John Shaffer, et al.
Mental Retardation and Developmental Disabilities Research Reviews|October 3, 2007
Epidemiology of Down syndromeStephanie L Sherman, Emily G Allen, Lora H Bean, et al.
Nucleic Acids Research|October 23, 2008
A novel procedure for genotyping of single nucleotide polymorphisms in trisomy with genomic DNA and the invader assayKelly J Duffy, Jack Littrell, Adam Locke, et al.
Journal of Genetic Counseling|May 25, 2017
Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X SyndromeVictoria Reines, Krista Charen, Tracie Rosser, et al.
Frontiers in Genetics|August 23, 2014
Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary studyEmily G Allen, Wendy E Grus, Sarayu Narayan, et al.
Journal of Human Genetics|November 21, 2009
Examination of FMR1 transcript and protein levels among 74 premutation carriersEmmanuel Peprah, Weiya He, Emily Allen, et al.
Genetic Epidemiology|December 29, 2015
Regionally Smoothed Meta-Analysis Methods for GWAS DatasetsFerdouse Begum, Monir H Sharker, Stephanie L Sherman, et al.
Pageof 13

Showing results (11-20 of 122) with videos related to

Sort By:
Pageof 13
Human Genetics|February 6, 2004
A study of the distributional characteristics of FMR1 transcript levels in 238 individualsEmily G Allen, Weiya He, Maneesha Yadav-Shah, et al.
G3 (Bethesda, Md.)|October 14, 2016
Genome-Wide Association Study of Meiotic Recombination PhenotypesFerdouse Begum, Reshmi Chowdhury, Vivian G Cheung, et al.
Genetic Epidemiology|January 30, 2004
A trisomic transmission disequilibrium testZhiying Xu, Kimberly F Kerstann, Stephanie L Sherman, et al.
American Journal of Human Genetics|November 20, 2004
Association between maternal age and meiotic recombination for trisomy 21Neil E Lamb, Kai Yu, John Shaffer, et al.
Mental Retardation and Developmental Disabilities Research Reviews|October 3, 2007
Epidemiology of Down syndromeStephanie L Sherman, Emily G Allen, Lora H Bean, et al.
Nucleic Acids Research|October 23, 2008
A novel procedure for genotyping of single nucleotide polymorphisms in trisomy with genomic DNA and the invader assayKelly J Duffy, Jack Littrell, Adam Locke, et al.
Journal of Genetic Counseling|May 25, 2017
Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X SyndromeVictoria Reines, Krista Charen, Tracie Rosser, et al.
Frontiers in Genetics|August 23, 2014
Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary studyEmily G Allen, Wendy E Grus, Sarayu Narayan, et al.
Journal of Human Genetics|November 21, 2009
Examination of FMR1 transcript and protein levels among 74 premutation carriersEmmanuel Peprah, Weiya He, Emily Allen, et al.
Genetic Epidemiology|December 29, 2015
Regionally Smoothed Meta-Analysis Methods for GWAS DatasetsFerdouse Begum, Monir H Sharker, Stephanie L Sherman, et al.
Pageof 13