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Nature Communications
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July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity
Aleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
June 30, 2023
2022 ACC/AHA guideline for the diagnosis and management of aortic disease: A report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines
, Eric M Isselbacher, Ourania Preventza, et al.
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Showing results (121-130 of 122) with videos related to
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Page
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This site can display upto 122 results.
Nature Communications
|
July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity
Aleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
June 30, 2023
2022 ACC/AHA guideline for the diagnosis and management of aortic disease: A report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines
, Eric M Isselbacher, Ourania Preventza, et al.
Page
of 13