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Connie Ens

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Orphanet Journal of Rare Diseases|August 21, 2025
Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics servicesTasha Wainstein, Cyrus Boelman, Connie Ens, et al.
Frontiers in Pediatrics|June 17, 2024
A mild phenotype associated with <i>KCNQ1</i> p.V205M mediated long QT syndrome in First Nations children of Northern British Columbia: effect of additional variants and considerations for managementSimona Bene Watts, Barbara Gauthier, Anders C Erickson, et al.
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Showing results (1-10 of 2) with videos related to

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Pageof 1
Orphanet Journal of Rare Diseases|August 21, 2025
Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics servicesTasha Wainstein, Cyrus Boelman, Connie Ens, et al.
Frontiers in Pediatrics|June 17, 2024
A mild phenotype associated with <i>KCNQ1</i> p.V205M mediated long QT syndrome in First Nations children of Northern British Columbia: effect of additional variants and considerations for managementSimona Bene Watts, Barbara Gauthier, Anders C Erickson, et al.
Pageof 1