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International Journal of Molecular Sciences
|
May 25, 2024
High-Throughput Genomics Identify Novel <i>FBN1/2</i> Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects
Gloria K E Zodanu, John H Hwang, Zubin Mehta, et al.
International Journal of Molecular Sciences
|
March 13, 2025
Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects
Gloria K E Zodanu, John H Hwang, Jordan Mudery, et al.
Cells
|
June 10, 2023
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in
Reiri Sono, Tania M Larrinaga, Alden Huang, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
August 13, 2021
Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome
Yan Zhao, Lee-Kai Wang, Ascia Eskin, et al.
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of 4
Search research articles
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Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 34 results.
International Journal of Molecular Sciences
|
May 25, 2024
High-Throughput Genomics Identify Novel <i>FBN1/2</i> Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects
Gloria K E Zodanu, John H Hwang, Zubin Mehta, et al.
International Journal of Molecular Sciences
|
March 13, 2025
Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects
Gloria K E Zodanu, John H Hwang, Jordan Mudery, et al.
Cells
|
June 10, 2023
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in
Reiri Sono, Tania M Larrinaga, Alden Huang, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
August 13, 2021
Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome
Yan Zhao, Lee-Kai Wang, Ascia Eskin, et al.
Page
of 4