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Fadi I Musfee

Showing results (11-20 of 15) with videos related to

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Genes|August 6, 2021
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United StatesOmobola O Oluwafemi, Fadi I Musfee, Laura E Mitchell, et al.
American Journal of Hypertension|July 26, 2020
Maternal Hypertension-Related Genotypes and Congenital Heart DefectsYunping Lei, Katherine L Ludorf, Xiao Yu, et al.
Epidemiology (Cambridge, Mass.)|March 28, 2023
Neighborhood-level Socioeconomic Position During Early Pregnancy and Risk of GastroschisisDayna 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 DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 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 StatesOmobola O Oluwafemi, Fadi I Musfee, Laura E Mitchell, et al.
American Journal of Hypertension|July 26, 2020
Maternal Hypertension-Related Genotypes and Congenital Heart DefectsYunping Lei, Katherine L Ludorf, Xiao Yu, et al.
Epidemiology (Cambridge, Mass.)|March 28, 2023
Neighborhood-level Socioeconomic Position During Early Pregnancy and Risk of GastroschisisDayna 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 DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Pageof 2