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August 6, 2021
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States
Omobola O Oluwafemi, Fadi I Musfee, Laura E Mitchell, et al.
American Journal of Hypertension
|
July 26, 2020
Maternal Hypertension-Related Genotypes and Congenital Heart Defects
Yunping Lei, Katherine L Ludorf, Xiao Yu, et al.
Epidemiology (Cambridge, Mass.)
|
March 28, 2023
Neighborhood-level Socioeconomic Position During Early Pregnancy and Risk of Gastroschisis
Dayna T Neo, Tania A Desrosiers, Chantel L Martin, et al.
Birth Defects Research
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July 13, 2023
Are individual-level risk factors for gastroschisis modified by neighborhood-level socioeconomic factors?
Dayna T Neo, Chantel L Martin, Suzan L Carmichael, et al.
American Journal of Human Genetics
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December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Yingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Genes
|
August 6, 2021
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States
Omobola O Oluwafemi, Fadi I Musfee, Laura E Mitchell, et al.
American Journal of Hypertension
|
July 26, 2020
Maternal Hypertension-Related Genotypes and Congenital Heart Defects
Yunping Lei, Katherine L Ludorf, Xiao Yu, et al.
Epidemiology (Cambridge, Mass.)
|
March 28, 2023
Neighborhood-level Socioeconomic Position During Early Pregnancy and Risk of Gastroschisis
Dayna T Neo, Tania A Desrosiers, Chantel L Martin, et al.
Birth Defects Research
|
July 13, 2023
Are individual-level risk factors for gastroschisis modified by neighborhood-level socioeconomic factors?
Dayna T Neo, Chantel L Martin, Suzan L Carmichael, et al.
American Journal of Human Genetics
|
December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Yingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Page
of 2