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Le Caignec, Cédric
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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