E-LIB Suche - Ergebnisse für: Blanchet, Patricia-Anne

1

Marcher vers l'humilité culturelle pédagogique à travers un..:

Blanchet, Patricia-Anne ; Lavoie, Constance ; Legault, Alexis..
Revista Educación, Política y Sociedad. 9 (2024) 2 - p. 14-50 , 2024

Link: https://doi.org/10.15366..

2

Ashtam Ntotacinan/Come Listen to Us: Theatricalization of L..:

Blanchet, Patricia-Anne
Theatre Research in Canada. 45 (2024) 1 - p. 56-79 , 2024

Link: https://doi.org/10.3138/..

3

Élaboration et appréciation d'un cours sur les perspectives..:

Lavoie, Constance ; Blanchet, Patricia-Anne ; O'Bomsawin, Suzie...
Journal of the Canadian Association for Curriculum Studies. 20 (2023) 1 - p. 65-87 , 2023

Link: https://doi.org/10.25071..

4

La discussion lexicale : une approche dialogique pour l'ana..:

Lavoie, Constance ; Blanchet, Patricia-Anne ; Pellerin, Martine
Lidil. , 2020

Link: https://doi.org/10.4000/..

5

Teaching Life Narratives in the Classroom: Strategies Based..:

Lavoie, Constance ; Blanchet, Patricia-Anne
Diaspora, Indigenous, and Minority Education. 12 (2018) 3 - p. 155-166 , 2018

Link: https://doi.org/10.1080/..

6

Expanding the phenotype of ASXL3‐related syndrome: A compre..:

Schirwani, Schaida ; Albaba, Shadi ; Carere, Deanna Alexis...
American Journal of Medical Genetics Part A. 185 (2021) 11 - p. 3446-3458 , 2021

Link: https://doi.org/10.1002/..

7

Report on three additional patients and genotype–phenotype ..:

Lemattre, Camille ; Imbert-Bouteille, Marion ; Gatinois, Vincent...
European Journal of Human Genetics. 27 (2019) 11 - p. 1692-1700 , 2019

Link: https://doi.org/10.1038/..

8

B3GAT3-related disorder with craniosynostosis and bone frag..:

Yauy, Kevin ; Tran Mau-Them, Frederic ; Willems, Marjolaine...
Genetics in Medicine. 20 (2018) 2 - p. 269-274 , 2018

Link: https://doi.org/10.1038/..

9

Mutations in RIT1 cause Noonan syndrome with possible juven..:

Cavé, Hélène ; Caye, Aurélie ; Ghedira, Nehla...
European Journal of Human Genetics. 24 (2016) 8 - p. 1124-1131 , 2016

Link: https://doi.org/10.1038/..

10

Treacher Collins syndrome: a clinical and molecular study b..:

Vincent, Marie ; Geneviève, David ; Ostertag, Agnès...
Genetics in Medicine. 18 (2016) 1 - p. 49-56 , 2016

Link: https://doi.org/10.1038/..

11

Cobblestone lissencephaly: neuropathological subtypes and c..:

Devisme, Louise ; Bouchet, Céline ; Gonzalès, Marie...
Brain. 135 (2012) 2 - p. 469-482 , 2012

Link: https://doi.org/10.1093/..

12

Molecular epidemiology of DFNB1 deafness in France:

Roux, Anne-Françoise ; Pallares-Ruiz, Nathalie ; Vielle, Anne...
BMC Medical Genetics. 5 (2004) 1 - p. , 2004

Link: https://doi.org/10.1186/..

13

Stable dicentric duplication‐deficiency chromosome 14 resul..:

Lefort, Geneviève ; Blanchet, Patricia ; Belgrade, Nabia...
American Journal of Medical Genetics. 113 (2002) 4 - p. 333-338 , 2002

Link: https://doi.org/10.1002/..

14

Multiplying recipients paired with oocyte donors optimizes ..:

de Ziegler, Dominique ; de Mouzon, Jacques ; Fauque, Patricia...
Fertility and Sterility. 95 (2011) 5 - p. 1633-1638 , 2011

Link: https://doi.org/10.1016/..

15

Norwegian killer whale movements reflect their different pr..:

Vogel, Emma F. ; Rikardsen, Audun H. ; Blanchet, Marie-Anne..
Polar Research. 43 (2024) - p. , 2024

Link: https://doi.org/10.33265..