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Blanchet, Patricia-Anne
255  Ergebnisse:
englisch X
Personensuche X
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1

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/..
 
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2

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/..
 
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3

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..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

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/..
 
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8

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/..
 
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9

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/..
 
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10

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/..
 
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11

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/..
 
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12

Prenatal diagnosis by trio exome sequencing in fetuses with..:

Tran Mau-Them, Frédéric ; Delanne, Julian ; Denommé-Pichon, Anne-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fgene.2023.1099995.  , 2023
Link: https://normandie-univ.h..
 
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13

Prenatal diagnosis by trio exome sequencing in fetuses with..:

Tran Mau-Them, Frédéric ; Delanne, Julian ; Denommé-Pichon, Anne-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fgene.2023.1099995.  , 2023
Link: https://normandie-univ.h..
 
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14

Prenatal diagnosis by trio exome sequencing in fetuses with..:

Tran Mau-Them, Frédéric ; Delanne, Julian ; Denommé-Pichon, Anne-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fgene.2023.1099995.  , 2023
Link: https://normandie-univ.h..
 
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15

Prenatal diagnosis by trio exome sequencing in fetuses with..:

Tran Mau-Them, Frédéric ; Delanne, Julian ; Denommé-Pichon, Anne-Sophie...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fgene.2023.1099995.  , 2023
Link: https://normandie-univ.h..
 
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