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

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..

3

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

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

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

4

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/..

5

Development and Assessment of a Teacher Education Course on..:

Lavoie, Constance ; Blanchet, Patricia-Anne ; Edward, Kara...
https://jcacs.journals.yorku.ca/index.php/jcacs/article/view/40755/36741. , 2024

Link: https://jcacs.journals.y..

6

The social and emotional foundations of learning:

Gotlieb, Rebecca J. M ; Hickey-Moody, Anna ; Güroğlu, Berna...
The International Science and Evidence-based Education Assessment: ISEE Assessment Working Group 3. , 2022

Link: https://unesdoc.unesco.o..

7

Les choix de contenus d'enseignement et d'évaluation de la ..:

Blanchet, Patricia-Anne
http://hdl.handle.net/11143/8730. , 2016

Link: http://hdl.handle.net/11..

8

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/..

9

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/..

10

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/..

11

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/..

12

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/..

13

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/..

14

Non-USH2A mutations in USH2 patients:

Besnard, Thomas ; Vaché, Christel ; Baux, David...
Human Mutation. 33 (2012) 3 - p. 504-510 , 2012

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

15

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/..