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Feger, Claire
56
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Online (56)
Mediatypes
Articles (Online) (12)
OpenAccess-fulltext (44)
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1
Pathogenic variants in KCNQ2 cause intellectual deficiency ..:
Mary, Laura
;
Nourisson, Elsa
;
Feger, Claire
...
American Journal of Medical Genetics Part A. 185 (2021) 6 - p. 1803-1815 , 2021
Link:
https://doi.org/10.1002/..
?
2
Integrative approach to interpret DYRK1A variants, leading ..:
Courraud, Jérémie
;
Chater-Diehl, Eric
;
Durand, Benjamin
...
Genetics in Medicine. 23 (2021) 11 - p. 2150-2159 , 2021
Link:
https://doi.org/10.1038/..
?
3
Novel mutations in NLGN3 causing autism spectrum disorder a..:
Quartier, Angélique
;
Courraud, Jérémie
;
Thi Ha, Thuong
...
Human Mutation. 40 (2019) 11 - p. 2021-2032 , 2019
Link:
https://doi.org/10.1002/..
?
4
Disease-causing variants in TCF4 are a frequent cause of in..:
Mary, Laura
;
Piton, Amélie
;
Schaefer, Elise
...
European Journal of Human Genetics. 26 (2018) 7 - p. 996-1006 , 2018
Link:
https://doi.org/10.1038/..
?
5
Intragenic FMR1 disease-causing variants: a significant mut..:
Quartier, Angélique
;
Poquet, Hélène
;
Gilbert-Dussardier, Brigitte
...
European Journal of Human Genetics. 25 (2017) 4 - p. 423-431 , 2017
Link:
https://doi.org/10.1038/..
?
6
Data set for describing the elaboration of a compatible Gat..:
Salim, Loubna
;
Feger, Claire
;
Busso, Didier
Data in Brief. 9 (2016) - p. 946-955 , 2016
Link:
https://doi.org/10.1016/..
?
7
Construction of a compatible Gateway-based co-expression ve..:
Salim, Loubna
;
Feger, Claire
;
Busso, Didier
Analytical Biochemistry. 512 (2016) - p. 110-113 , 2016
Link:
https://doi.org/10.1016/..
?
8
An Integrated Diagnosis Strategy for Congenital Myopathies:
Böhm, Johann
;
Vasli, Nasim
;
Malfatti, Edoardo
...
PLoS ONE. 8 (2013) 6 - p. e67527 , 2013
Link:
https://doi.org/10.1371/..
?
9
SLITRK2 variants associated with neurodevelopmental disorde..:
El Chehadeh, Salima
;
Han, Kyung Ah
;
Kim, Dongwook
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287327/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
10
SLITRK2 variants associated with neurodevelopmental disorde..:
El Chehadeh, Salima
;
Han, Kyung Ah
;
Kim, Dongwook
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-022-31566-z. , 2022
Link:
https://hal.science/hal-..
?
11
SLITRK2 variants associated with neurodevelopmental disorde..:
El Chehadeh, Salima
;
Han, Kyung Ah
;
Kim, Dongwook
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-022-31566-z. , 2022
Link:
https://hal.science/hal-..
?
12
SLITRK2 variants associated with neurodevelopmental disorde..:
El Chehadeh, Salima
;
Han, Kyung Ah
;
Kim, Dongwook
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-022-31566-z. , 2022
Link:
https://hal.science/hal-..
?
13
Integrative approach to interpret DYRK1A variants, leading ..:
Courraud, Jeremie
;
Chater-Diehl, Eric
;
Durand, Benjamin
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01263-1. , 2021
Link:
https://hal.science/hal-..
?
14
Integrative approach to interpret DYRK1A variants, leading ..:
Courraud, Jeremie
;
Chater-Diehl, Eric
;
Durand, Benjamin
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01263-1. , 2021
Link:
https://hal.science/hal-..
?
15
Integrative approach to interpret DYRK1A variants, leading ..:
Courraud, Jeremie
;
Chater-Diehl, Eric
;
Durand, Benjamin
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01263-1. , 2021
Link:
https://hal.science/hal-..
1-15
