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Thuong T Ha

Showing results (1-10 of 7) with videos related to

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American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Neuromuscular Disorders : NMD|May 20, 2023
Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysisRoula Ghaoui, Thuong T Ha, Jennifer Kerkhof, et al.
Human Mutation|April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disabilityMichael J Field, Raman Kumar, Anna Hackett, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Nature Medicine|July 10, 2023
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Nature Medicine|January 19, 2023
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Human Genomics|November 13, 2025
Atypical presentations of fetal polycystic kidney disease demonstrates the utility of a genomic autopsy for accurate post-mortem diagnosesMahalia S B Frank, Melissa K Bennett, Thuong T Ha, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Neuromuscular Disorders : NMD|May 20, 2023
Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysisRoula Ghaoui, Thuong T Ha, Jennifer Kerkhof, et al.
Human Mutation|April 13, 2021
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disabilityMichael J Field, Raman Kumar, Anna Hackett, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Nature Medicine|July 10, 2023
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Nature Medicine|January 19, 2023
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Human Genomics|November 13, 2025
Atypical presentations of fetal polycystic kidney disease demonstrates the utility of a genomic autopsy for accurate post-mortem diagnosesMahalia S B Frank, Melissa K Bennett, Thuong T Ha, et al.
Pageof 1