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Page 1
DOORS syndrome and a recurrent truncating ATP6V1B2 variant.
Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich K, Dabir T, Vind-Kezunovic D, White SM, Zadori D, Castiglioni C, Tranebjærg L, Tørring PM, Blair E, Wisniewska M, Camurri MV, van Bever Y, Molidperee S, Taylor J, Dionne-Laporte A, Sisodiya SM, Hennekam RCM, Campeau PM. Beauregard-Lacroix E, et al. Among authors: tardif j. Genet Med. 2021 Jan;23(1):149-154. doi: 10.1038/s41436-020-00950-9. Epub 2020 Sep 2. Genet Med. 2021. PMID: 32873933 Free article.
Expression signature of the Leigh syndrome French-Canadian type.
Bchetnia M, Tardif J, Morin C, Laprise C. Bchetnia M, et al. Among authors: tardif j. Mol Genet Metab Rep. 2022 Feb 5;30:100847. doi: 10.1016/j.ymgmr.2022.100847. eCollection 2022 Mar. Mol Genet Metab Rep. 2022. PMID: 35242578 Free PMC article.
Costing analysis of a point-of-care drug checking program in Rhode Island.
Cepeda JA, Thompson E, Ujeneza M, Tardif J, Walsh T, Morales A, Rosen JG, Green TC, Park JN. Cepeda JA, et al. Among authors: tardif j. Drug Alcohol Depend. 2023 Dec 1;253:111028. doi: 10.1016/j.drugalcdep.2023.111028. Epub 2023 Nov 15. Drug Alcohol Depend. 2023. PMID: 38000322
Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant.
Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich K, Dabir T, Vind-Kezunovic D, White SM, Zadori D, Castiglioni C, Tranebjærg L, Tørring PM, Blair E, Wisniewska M, Camurri MV, van Bever Y, Molidperee S, Taylor J, Dionne-Laporte A, Sisodiya SM, Hennekam RCM, Campeau PM. Beauregard-Lacroix E, et al. Among authors: tardif j. Genet Med. 2021 Jan;23(1):237. doi: 10.1038/s41436-020-00969-y. Genet Med. 2021. PMID: 32934366 Free article. No abstract available.
23 results