Zobrazeno 1 - 10
of 465
pro vyhledávání: '"Langlois Sylvie"'
Autor:
Gomez, Ricardo Santiago, El Mouatani, Ahmed, Duarte-Andrade, Filipe Fideles, Pereira, Thais dos Santos Fontes, Guimarães, Letícia Martins, Gayden, Tenzin, Faury, Damien, Nakada, Emily M., Langlois, Sylvie, Sinnett, Daniel, de Castro, Wagner Henriques, Diniz, Marina Gonçalves, Jabado, Nada, Gomes, Carolina Cavalieri
Publikováno v:
In Modern Pathology February 2024 37(2)
Autor:
Marra Marco, Lemyre Emmanuelle, Langlois Sylvie, Lam Wan L, Eydoux Patrice, Delaney Allen, Coe Bradley P, Chénier Sébastien, Chan Susanna, Chai David, Montpetit Alexandre, Tucker Tracy, Qian Hong, Rouleau Guy A, Vincent David, Michaud Jacques L, Friedman Jan M
Publikováno v:
BMC Medical Genomics, Vol 4, Iss 1, p 25 (2011)
Abstract Background Clinical laboratories are adopting array genomic hybridization as a standard clinical test. A number of whole genome array genomic hybridization platforms are available, but little is known about their comparative performance in a
Externí odkaz:
https://doaj.org/article/70ce637817d340d7b384a4f269306f8d
Autor:
Li H Irene, Lemyre Emmanuelle, Langlois Sylvie, Gibson William T, Flibotte Stephane, Delaney Allen D, Chai David, Chan Susanna, Boerkoel Cornelius, Birch Patricia, Baross Agnes, Armstrong Linlea, Arbour Laura, Adam Shelin, Friedman JM, MacLeod Patrick, Mathers Joan, Michaud Jacques L, McGillivray Barbara C, Patel Millan S, Qian Hong, Rouleau Guy A, Van Allen Margot I, Yong Siu-Li, Zahir Farah R, Eydoux Patrice, Marra Marco A
Publikováno v:
BMC Genomics, Vol 10, Iss 1, p 526 (2009)
Abstract Background Array genomic hybridization is being used clinically to detect pathogenic copy number variants in children with intellectual disability and other birth defects. However, there is no agreement regarding the kind of array, the distr
Externí odkaz:
https://doaj.org/article/f4c731e301114efe9e880d23b03d48d4
Autor:
Kennedy Giulia, Go Anne, Fernandes Nicole, Brown-John Mabel, Birch Patricia, Cao Manqiu, Ally Adrian, Asano Jennifer, Chan Susanna Y, Qian Hong, Flibotte Stephane, Nayar Tarun, Li H Irene, Delaney Allen D, Baross Ágnes, Langlois Sylvie, Eydoux Patrice, Friedman JM, Marra Marco A
Publikováno v:
BMC Bioinformatics, Vol 8, Iss 1, p 368 (2007)
Abstract Background Genomic deletions and duplications are important in the pathogenesis of diseases, such as cancer and mental retardation, and have recently been shown to occur frequently in unaffected individuals as polymorphisms. Affymetrix GeneC
Externí odkaz:
https://doaj.org/article/cb041a68db54480bb203430381078a12
Autor:
Tsai, Harrison K., Gogakos, Tasos, Lip, Va, Tsai, Jonathan M., Li, Yen-Der, Fisch, Adam S., Weiss, Jonathan, Yang, Weiping, Grimmett, Leslie, DiToro, Daniel, Schaefer, Eva J., Lindsley, R. Coleman, Tran, Thai Hoa, Caron, Maxime, Langlois, Sylvie, Sinnett, Daniel, Pikman, Yana, Nardi, Valentina, Kim, Annette S., Silverman, Lewis B., Harris, Marian H.
Publikováno v:
In The Journal of Molecular Diagnostics June 2023
Autor:
Tran, Thai Hoa *, Langlois, Sylvie, Meloche, Caroline, Caron, Maxime, Saint-Onge, Pascal, Rouette, Alexandre, Bataille, Alain R., Jimenez-Cortes, Camille, Sontag, Thomas, Bittencourt, Henrique, Laverdière, Caroline, Lavallée, Vincent-Philippe, Leclerc, Jean-Marie, Cole, Peter D., Gennarini, Lisa M., Kahn, Justine M., Kelly, Kara M., Michon, Bruno, Santiago, Raoul, Stevenson, Kristen E., Welch, Jennifer J.G., Schroeder, Kaitlin M., Koch, Victoria, Cellot, Sonia, Silverman, Lewis B., Sinnett, Daniel *
Publikováno v:
In Blood Advances 22 February 2022 6(4):1329-1341
Publikováno v:
In Journal of Obstetrics and Gynaecology Canada January 2021 43(1):140-157
Publikováno v:
In Journal of Obstetrics and Gynaecology Canada January 2021 43(1):124-139
Autor:
Zwingerman, Rhonda, Langlois, Sylvie
Publikováno v:
In Journal of Obstetrics and Gynaecology Canada November 2020 42(11):1444-1451
Autor:
Zwingerman, Rhonda, Langlois, Sylvie
Publikováno v:
In Journal of Obstetrics and Gynaecology Canada November 2020 42(11):1437-1443