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Jacob Munro

Showing results (21-30 of 25) with videos related to

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Brain Communications|November 21, 2025
Novel, complex configurations of the <i>MARCHF6</i> repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsyMark F Bennett, Mark A Corbett, Thessa Kroes, et al.
Nature Communications|June 9, 2021
Maternal iron deficiency perturbs embryonic cardiovascular development in miceJacinta I Kalisch-Smith, Nikita Ved, Dorota Szumska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
Orphanet Journal of Rare Diseases|August 2, 2024
Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is agelessMathew Wallis, Simon D Bodek, Jacob Munro, et al.
Cell|March 21, 2026
The E3-ome gene-centric compendium reveals the human E3 ligase landscapeNgee Kiat Chua, Tania J González-Robles, Cameron J Reddington, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Brain Communications|November 21, 2025
Novel, complex configurations of the <i>MARCHF6</i> repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsyMark F Bennett, Mark A Corbett, Thessa Kroes, et al.
Nature Communications|June 9, 2021
Maternal iron deficiency perturbs embryonic cardiovascular development in miceJacinta I Kalisch-Smith, Nikita Ved, Dorota Szumska, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
Orphanet Journal of Rare Diseases|August 2, 2024
Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is agelessMathew Wallis, Simon D Bodek, Jacob Munro, et al.
Cell|March 21, 2026
The E3-ome gene-centric compendium reveals the human E3 ligase landscapeNgee Kiat Chua, Tania J González-Robles, Cameron J Reddington, et al.
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