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Emily G Allen

Showing results (41-50 of 59) with videos related to

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Public Health Reports (Washington, D.C. : 1974)|January 24, 2007
The National Down Syndrome Project: design and implementationSallie B Freeman, Emily G Allen, Cindy L Oxford-Wright, et al.
Cell Reports|December 13, 2018
Ten-Eleven Translocation Proteins Modulate the Response to Environmental Stress in MiceYing Cheng, Miao Sun, Li Chen, et al.
Human Molecular Genetics|December 10, 2019
Ethnicity-specific and overlapping alterations of brain hydroxymethylome in Alzheimer's diseaseLixia Qin, Qian Xu, Ziyi Li, et al.
Frontiers in Aging Neuroscience|January 23, 2023
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndromeAndrea Elias-Mas, Miriam Potrony, Jaume Bague, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome ProjectSallie B Freeman, Lora H Bean, Emily G Allen, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome ProjectNaTasha D Hollis, Emily G Allen, Tiffany Renee Oliver, et al.
Human Molecular Genetics|April 16, 2019
Rare variants in MYH15 modify amyotrophic lateral sclerosis riskHyerim Kim, Junghwa Lim, Han Bao, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 12, 2011
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome ProjectLora J H Bean, Emily G Allen, Stuart W Tinker, et al.
Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.
Molecular Genetics & Genomic Medicine|July 19, 2022
Descriptive analysis of seizures and comorbidities associated with fragile X syndromeIgor Albizua, Krista Charen, Lisa Shubeck, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Public Health Reports (Washington, D.C. : 1974)|January 24, 2007
The National Down Syndrome Project: design and implementationSallie B Freeman, Emily G Allen, Cindy L Oxford-Wright, et al.
Cell Reports|December 13, 2018
Ten-Eleven Translocation Proteins Modulate the Response to Environmental Stress in MiceYing Cheng, Miao Sun, Li Chen, et al.
Human Molecular Genetics|December 10, 2019
Ethnicity-specific and overlapping alterations of brain hydroxymethylome in Alzheimer's diseaseLixia Qin, Qian Xu, Ziyi Li, et al.
Frontiers in Aging Neuroscience|January 23, 2023
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndromeAndrea Elias-Mas, Miriam Potrony, Jaume Bague, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome ProjectSallie B Freeman, Lora H Bean, Emily G Allen, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome ProjectNaTasha D Hollis, Emily G Allen, Tiffany Renee Oliver, et al.
Human Molecular Genetics|April 16, 2019
Rare variants in MYH15 modify amyotrophic lateral sclerosis riskHyerim Kim, Junghwa Lim, Han Bao, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 12, 2011
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome ProjectLora J H Bean, Emily G Allen, Stuart W Tinker, et al.
Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.
Molecular Genetics & Genomic Medicine|July 19, 2022
Descriptive analysis of seizures and comorbidities associated with fragile X syndromeIgor Albizua, Krista Charen, Lisa Shubeck, et al.
Pageof 6