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Le Caignec, Cédric
352
results:
Search for persons
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Format
Online (352)
Mediatypes
Articles (Online) (83)
OpenAccess-fulltext (269)
Languages
english (343)
french (4)
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?
1
Author Correction: Possible association of 16p11.2 copy num..:
Giannuzzi, Giuliana
;
Chatron, Nicolas
;
Mannik, Katrin
...
npj Genomic Medicine. 8 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
2
Assortative mating and parental genetic relatedness contrib..:
Smolen, Corrine
;
Jensen, Matthew
;
Dyer, Lisa
...
The American Journal of Human Genetics. 110 (2023) 12 - p. 2015-2028 , 2023
Link:
https://doi.org/10.1016/..
?
3
Cat eye syndrome: Clinical, cytogenetics and familial findi..:
Jedraszak, Guillaume
;
Jobic, Florence
;
Receveur, Aline
...
American Journal of Medical Genetics Part A. 194 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1002/..
?
4
Antenatal ultrasound features of isolated recurrent copy nu..:
Courdier, Cécile
;
Boudjarane, John
;
Malan, Valérie
...
Prenatal Diagnosis. 43 (2023) 6 - p. 734-745 , 2023
Link:
https://doi.org/10.1002/..
?
5
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/..
?
6
Possible association of 16p11.2 copy number variation with ..:
Giannuzzi, Giuliana
;
Chatron, Nicolas
;
Mannik, Katrin
...
npj Genomic Medicine. 7 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
7
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/..
?
8
Primrose syndrome: a phenotypic comparison of patients with..:
Juven, Aurélien
;
Nambot, Sophie
;
Piton, Amélie
...
European Journal of Human Genetics. 28 (2020) 8 - p. 1044-1055 , 2020
Link:
https://doi.org/10.1038/..
?
9
Author Correction: A framework to identify contributing gen..:
Tabet, Anne-Claude
;
Rolland, Thomas
;
Ducloy, Marie
...
npj Genomic Medicine. 4 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
10
Fryns type mesomelic dysplasia of the upper limbs caused by..:
Le Caignec, Cédric
;
Pichon, Olivier
;
Briand, Annaig
...
European Journal of Human Genetics. 28 (2019) 3 - p. 324-332 , 2019
Link:
https://doi.org/10.1038/..
?
11
Correction: Variants in MED12L, encoding a subunit of the M..:
Nizon, Mathilde
;
Laugel, Vincent
;
Flanigan, Kevin M.
...
Genetics in Medicine. 21 (2019) 11 - p. 2663 , 2019
Link:
https://doi.org/10.1038/..
?
12
Oro-dental phenotype in patients with RUNX2 duplication:
Merametdjian, Laure
;
Prud'Homme, Tony
;
Le Caignec, Cédric
..
European Journal of Medical Genetics. 62 (2019) 2 - p. 85-89 , 2019
Link:
https://doi.org/10.1016/..
?
13
Pathogenic variants in USP7 cause a neurodevelopmental diso..:
Fountain, Michael D.
;
Oleson, David S.
;
Rech, Megan E.
...
Genetics in Medicine. 21 (2019) 8 - p. 1797-1807 , 2019
Link:
https://doi.org/10.1038/..
?
14
RPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with ..:
Le Caignec, Cedric
;
Ory, Benjamin
;
Lamoureux, François
...
The American Journal of Human Genetics. 105 (2019) 5 - p. 1040-1047 , 2019
Link:
https://doi.org/10.1016/..
?
15
Variants in MED12L, encoding a subunit of the mediator kina..:
Nizon, Mathilde
;
Laugel, Vincent
;
Flanigan, Kevin M.
...
Genetics in Medicine. 21 (2019) 12 - p. 2713-2722 , 2019
Link:
https://doi.org/10.1038/..
1-15