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Landais, Emilie
249
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Online (249)
Mediatypes
Articles (Online) (32)
OpenAccess-fulltext (217)
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english (232)
french (11)
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?
1
P199: Novel homozygous GLDC variants causing late-onset gly..:
Huynh, Minh-Tuan
;
Landais, Emilie
;
De Sainte Agathe, Jean-Madeleine
..
Genetics in Medicine Open. 1 (2023) 1 - p. 100228 , 2023
Link:
https://doi.org/10.1016/..
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2
Novel homozygous GLDC variant causing late-onset glycine en..:
Huynh, Minh-Tuan
;
Landais, Emilie
;
Agathe, Jean-Madeleine De Sainte
...
Molecular Genetics and Metabolism Reports. 34 (2023) - p. 100959 , 2023
Link:
https://doi.org/10.1016/..
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3
1p36 deletion syndrome: Review and mapping with further cha..:
Jacquin, Clémence
;
Landais, Emilie
;
Poirsier, Céline
...
American Journal of Medical Genetics Part A. 191 (2022) 2 - p. 445-458 , 2022
Link:
https://doi.org/10.1002/..
?
4
Clinical and genomic delineation of the new proximal 19p13...:
Jouret, Guillaume
;
Egloff, Matthieu
;
Landais, Emilie
...
American Journal of Medical Genetics Part A. 191 (2022) 1 - p. 52-63 , 2022
Link:
https://doi.org/10.1002/..
?
5
Complete lung agenesis caused by complex genomic rearrangem..:
Melo, Uirá Souto
;
Piard, Juliette
;
Fischer-Zirnsak, Björn
...
Human Genetics. 140 (2021) 10 - p. 1459-1469 , 2021
Link:
https://doi.org/10.1007/..
?
6
A pure familial 6q15q21 split duplication associated with o..:
Landais, Emilie
;
Leroy, Camille
;
Kleinfinger, Pascale
...
American Journal of Medical Genetics Part A. 167 (2015) 6 - p. 1275-1284 , 2015
Link:
https://doi.org/10.1002/..
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7
Porn studies et études de la pornographie en sciences humai..:
Landais, Émilie
Questions de communication. , 2014
Link:
https://doi.org/10.4000/..
?
8
Report on 3 patients with 12p duplication including GRIN2B:
Poirsier, Celine
;
Landais, Emilie
;
Bednarek, Nathalie
...
European Journal of Medical Genetics. 57 (2014) 5 - p. 185-194 , 2014
Link:
https://doi.org/10.1016/..
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9
Frédéric Darbellay, éd., La circulation des savoirs. Interd..:
Landais, Émilie
Questions de communication. , 2014
Link:
https://doi.org/10.4000/..
?
10
Loss of function of KIAA2022 causes mild to severe intellec..:
Van Maldergem, Lionel
;
Hou, Qingming
;
Kalscheuer, Vera M.
...
Human Molecular Genetics. 22 (2013) 16 - p. 3306-3314 , 2013
Link:
https://doi.org/10.1093/..
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11
Bipolar affective disorder and early dementia onset in a ma..:
Vucurovic, Ksenija
;
Landais, Emilie
;
Delahaigue, Cécile
...
European Journal of Medical Genetics. 55 (2012) 11 - p. 625-629 , 2012
Link:
https://doi.org/10.1016/..
?
12
Éleni Mitropoulou, Nicole Pignier, coords, « De l'interacti..:
Landais, Émilie
Questions de communication. , 2012
Link:
https://doi.org/10.4000/..
?
13
Clinical and molecular characterization of 17q21.31 microde..:
Dubourg, Christèle
;
Sanlaville, Damien
;
Doco-Fenzy, Martine
...
European Journal of Medical Genetics. 54 (2011) 2 - p. 144-151 , 2011
Link:
https://doi.org/10.1016/..
?
14
A 5.3Mb deletion in chromosome 18q12.3 as the smallest regi..:
Bouquillon, Sonia
;
Andrieux, Joris
;
Landais, Emilie
...
European Journal of Medical Genetics. 54 (2011) 2 - p. 194-197 , 2011
Link:
https://doi.org/10.1016/..
?
15
Genotype–phenotype correlation in four 15q24 deleted patien..:
Andrieux, Joris
;
Dubourg, Christèle
;
Rio, Marlène
...
American Journal of Medical Genetics Part A. 149A (2009) 12 - p. 2813-2819 , 2009
Link:
https://doi.org/10.1002/..
1-15