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Showing results (161-170 of 234) with videos related to

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American Journal of Medical Genetics. Part A|September 8, 2005
Screening for new MTHFR polymorphisms and NTD riskValerie B O'Leary, James L Mills, Anne Parle-McDermott, et al.
Nature Genetics|October 1, 1996
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%C Oddoux, J P Struewing, C M Clayton, et al.
Scientific Reports|December 10, 2017
The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within IrelandEdmund Gilbert, Seamus O'Reilly, Michael Merrigan, et al.
The American Journal of Clinical Nutrition|March 23, 2018
Lifestyle, metabolite, and genetic determinants of formate concentrations in a cross-sectional study in young, healthy adultsJohn T Brosnan, James L Mills, Per M Ueland, et al.
Plos One|December 8, 2017
Copy number variants in Ebstein anomalyAndreas Giannakou, Robert J Sicko, Wei Zhang, et al.
Molecular Human Reproduction|August 27, 2005
A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy lossAnne Parle-McDermott, Faith Pangilinan, James L Mills, et al.
Human Mutation|September 25, 2009
A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiencyAnne Parle-McDermott, Faith Pangilinan, Kirsty K O'Brien, et al.
Journal of Human Genetics|May 6, 2003
Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defectsAnne Parle-McDermott, James L Mills, Peadar N Kirke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Novel copy-number variants in a population-based investigation of classic heterotaxyShannon L Rigler, Denise M Kay, Robert J Sicko, et al.
Plos One|October 28, 2016
Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development PathwaysRobert J Sicko, Marilyn L Browne, Shannon L Rigler, et al.
Pageof 24

Showing results (161-170 of 234) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics. Part A|September 8, 2005
Screening for new MTHFR polymorphisms and NTD riskValerie B O'Leary, James L Mills, Anne Parle-McDermott, et al.
Nature Genetics|October 1, 1996
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%C Oddoux, J P Struewing, C M Clayton, et al.
Scientific Reports|December 10, 2017
The Irish DNA Atlas: Revealing Fine-Scale Population Structure and History within IrelandEdmund Gilbert, Seamus O'Reilly, Michael Merrigan, et al.
The American Journal of Clinical Nutrition|March 23, 2018
Lifestyle, metabolite, and genetic determinants of formate concentrations in a cross-sectional study in young, healthy adultsJohn T Brosnan, James L Mills, Per M Ueland, et al.
Plos One|December 8, 2017
Copy number variants in Ebstein anomalyAndreas Giannakou, Robert J Sicko, Wei Zhang, et al.
Molecular Human Reproduction|August 27, 2005
A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy lossAnne Parle-McDermott, Faith Pangilinan, James L Mills, et al.
Human Mutation|September 25, 2009
A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiencyAnne Parle-McDermott, Faith Pangilinan, Kirsty K O'Brien, et al.
Journal of Human Genetics|May 6, 2003
Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defectsAnne Parle-McDermott, James L Mills, Peadar N Kirke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Novel copy-number variants in a population-based investigation of classic heterotaxyShannon L Rigler, Denise M Kay, Robert J Sicko, et al.
Plos One|October 28, 2016
Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development PathwaysRobert J Sicko, Marilyn L Browne, Shannon L Rigler, et al.
Pageof 24