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Stephanie L Sherman

Showing results (31-40 of 122) with videos related to

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Genetic Epidemiology|March 22, 2008
Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severityJessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, et al.
Journal of Assisted Reproduction and Genetics|November 29, 2022
The diagnostic experience of women with fragile X-associated primary ovarian insufficiency (FXPOI)Bonnie Poteet, Nadia Ali, Cecelia Bellcross, et al.
Statistics in Biosciences|May 4, 2010
A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical OutcomesMichael P Epstein, Jessica E Hunter, Emily G Allen, et al.
American Journal of Human Genetics|October 7, 2009
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNABradford Coffee, Krayton Keith, Igor Albizua, et al.
Birth Defects Research|December 24, 2021
Co-occurrence of congenital anomalies by maternal race/ethnicity among infants and fetuses with Down syndrome, 2013-2017: A U.S. population-based analysisErin B Stallings, Jennifer L Isenburg, Dominique Heinke, et al.
Human Molecular Genetics|August 24, 2012
Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in miceCuiling Lu, Li Lin, Huiping Tan, et al.
American Journal of Medical Genetics. Part A|September 21, 2016
Importance of a specialty clinic for individuals with fragile X syndromeJeannie Visootsak, Sharon A Kidd, Tovi Anderson, et al.
Journal of Genetic Counseling|March 31, 2021
Men with an FMR1 premutation and their health education needsMatthew B Walsh, Krista Charen, Lisa Shubeck, et al.
Prenatal Diagnosis|July 1, 2011
Fragile X analysis of 1112 prenatal samples from 1991 to 2010Sarah L Nolin, Anne Glicksman, Xiaohua Ding, et al.
Human Reproduction (Oxford, England)|May 10, 2005
CYP17 genotype predicts serum hormone levels among pre-menopausal womenChanley M Small, Michele Marcus, Stephanie L Sherman, et al.
Pageof 13

Showing results (31-40 of 122) with videos related to

Sort By:
Pageof 13
Genetic Epidemiology|March 22, 2008
Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severityJessica Ezzell Hunter, Michael P Epstein, Stuart W Tinker, et al.
Journal of Assisted Reproduction and Genetics|November 29, 2022
The diagnostic experience of women with fragile X-associated primary ovarian insufficiency (FXPOI)Bonnie Poteet, Nadia Ali, Cecelia Bellcross, et al.
Statistics in Biosciences|May 4, 2010
A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical OutcomesMichael P Epstein, Jessica E Hunter, Emily G Allen, et al.
American Journal of Human Genetics|October 7, 2009
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNABradford Coffee, Krayton Keith, Igor Albizua, et al.
Birth Defects Research|December 24, 2021
Co-occurrence of congenital anomalies by maternal race/ethnicity among infants and fetuses with Down syndrome, 2013-2017: A U.S. population-based analysisErin B Stallings, Jennifer L Isenburg, Dominique Heinke, et al.
Human Molecular Genetics|August 24, 2012
Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in miceCuiling Lu, Li Lin, Huiping Tan, et al.
American Journal of Medical Genetics. Part A|September 21, 2016
Importance of a specialty clinic for individuals with fragile X syndromeJeannie Visootsak, Sharon A Kidd, Tovi Anderson, et al.
Journal of Genetic Counseling|March 31, 2021
Men with an FMR1 premutation and their health education needsMatthew B Walsh, Krista Charen, Lisa Shubeck, et al.
Prenatal Diagnosis|July 1, 2011
Fragile X analysis of 1112 prenatal samples from 1991 to 2010Sarah L Nolin, Anne Glicksman, Xiaohua Ding, et al.
Human Reproduction (Oxford, England)|May 10, 2005
CYP17 genotype predicts serum hormone levels among pre-menopausal womenChanley M Small, Michele Marcus, Stephanie L Sherman, et al.
Pageof 13