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A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
Nat Med. 2010 Oct;16(10):1157-60. doi: 10.1038/nm.2216. Epub 2010 Sep 26.
Nat Med. 2010.
PMID: 20871611
A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study.
Lapointe J, Dorval M, Chiquette J, Joly Y, Guertin JR, Laberge M, Gekas J, Hébert J, Pomey MP, Cruz-Marino T, Touhami O, Blanchet Saint-Pierre A, Gagnon S, Bouchard K, Rhéaume J, Boisvert K, Brousseau C, Castonguay L, Fortier S, Gosselin I, Lachapelle P, Lavoie S, Poirier B, Renaud MC, Ruizmangas MG, Sebastianelli A, Roy S, Côté M, Racine MM, Roy MC, Côté N, Brisson C, Charette N, Faucher V, Leblanc J, Dubeau MÈ, Plante M, Desbiens C, Beaumont M, Simard J, Nabi H.
Lapointe J, et al. Among authors: boisvert k.
Cancers (Basel). 2021 May 31;13(11):2729. doi: 10.3390/cancers13112729.
Cancers (Basel). 2021.
PMID: 34072979
Free PMC article.
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CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems.
Chénier S, Yoon G, Argiropoulos B, Lauzon J, Laframboise R, Ahn JW, Ogilvie CM, Lionel AC, Marshall CR, Vaags AK, Hashemi B, Boisvert K, Mathonnet G, Tihy F, So J, Scherer SW, Lemyre E, Stavropoulos DJ.
Chénier S, et al. Among authors: boisvert k.
J Neurodev Disord. 2014;6(1):9. doi: 10.1186/1866-1955-6-9. Epub 2014 Apr 22.
J Neurodev Disord. 2014.
PMID: 24834135
Free PMC article.
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RETIRED: The physician expert in legal proceedings.
Owolabi T, Vilos G, Carson G; MEDICO-LEGAL COMMITTEE.
Owolabi T, et al.
J Obstet Gynaecol Can. 2006 Oct;28(10):913-915. doi: 10.1016/S1701-2163(16)32272-1.
J Obstet Gynaecol Can. 2006.
PMID: 17140510
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