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Stephanie L Sherman

Showing results (21-30 of 122) with videos related to

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Human Molecular Genetics|December 10, 2019
Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypesIgor Albizua, Pankaj Chopra, Stephanie L Sherman, et al.
American Journal of Medical Genetics. Part A|July 17, 2009
Investigation of factors associated with paternal nondisjunction of chromosome 21Tiffany Renee Oliver, Archit Bhise, Eleanor Feingold, et al.
Plos Genetics|September 19, 2009
Genetic analysis of variation in human meiotic recombinationReshmi Chowdhury, Philippe R J Bois, Eleanor Feingold, et al.
Journal of Theory Construction & Testing|September 19, 2025
A Parent-Response Screening Inventory for Fragile X Syndrome: Development & Testing with an International SampleVanessa A Johnson, Yolanda M Powell-Young, Bradley Brossman, et al.
Behavior Genetics|November 22, 2011
The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritanceJessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, et al.
International Journal of Hygiene and Environmental Health|September 15, 2019
The association between maternal occupation and down syndrome: A report from the national Down syndrome projectColleen Keen, Jessica Ezzell Hunter, Emily Graves Allen, et al.
Menopause (New York, N.Y.)|August 24, 2016
Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI)Heather S Hipp, Krista H Charen, Jessica B Spencer, et al.
Annals of Human Genetics|July 6, 2010
Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African populationEmmanuel K Peprah, Emily G Allen, Scott M Williams, et al.
Human Genetics|June 14, 2020
Study of telomere length in men who carry a fragile X premutation or full mutation alleleIgor Albizua, Pankaj Chopra, Emily G Allen, et al.
American Journal of Human Genetics|May 7, 2002
Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size rangeAmy K Sullivan, Dana C Crawford, Elizabeth H Scott, et al.
Pageof 13

Showing results (21-30 of 122) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|December 10, 2019
Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypesIgor Albizua, Pankaj Chopra, Stephanie L Sherman, et al.
American Journal of Medical Genetics. Part A|July 17, 2009
Investigation of factors associated with paternal nondisjunction of chromosome 21Tiffany Renee Oliver, Archit Bhise, Eleanor Feingold, et al.
Plos Genetics|September 19, 2009
Genetic analysis of variation in human meiotic recombinationReshmi Chowdhury, Philippe R J Bois, Eleanor Feingold, et al.
Journal of Theory Construction & Testing|September 19, 2025
A Parent-Response Screening Inventory for Fragile X Syndrome: Development & Testing with an International SampleVanessa A Johnson, Yolanda M Powell-Young, Bradley Brossman, et al.
Behavior Genetics|November 22, 2011
The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritanceJessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, et al.
International Journal of Hygiene and Environmental Health|September 15, 2019
The association between maternal occupation and down syndrome: A report from the national Down syndrome projectColleen Keen, Jessica Ezzell Hunter, Emily Graves Allen, et al.
Menopause (New York, N.Y.)|August 24, 2016
Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI)Heather S Hipp, Krista H Charen, Jessica B Spencer, et al.
Annals of Human Genetics|July 6, 2010
Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African populationEmmanuel K Peprah, Emily G Allen, Scott M Williams, et al.
Human Genetics|June 14, 2020
Study of telomere length in men who carry a fragile X premutation or full mutation alleleIgor Albizua, Pankaj Chopra, Emily G Allen, et al.
American Journal of Human Genetics|May 7, 2002
Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size rangeAmy K Sullivan, Dana C Crawford, Elizabeth H Scott, et al.
Pageof 13