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Hervé, Bérénice
125
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Online (125)
Mediatypes
Articles (Online) (27)
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1
Shifting the landscape: Dominant C‐terminal rare missense F..:
Jordan, Pénélope
;
Verebi, Camille
;
Hervé, Bérénice
...
Clinical Genetics. 106 (2024) 1 - p. 102-108 , 2024
Link:
https://doi.org/10.1111/..
?
2
Revisiting GDF9 variants in primary ovarian insufficiency: ..:
Jordan, Pénélope
;
Verebi, Camille
;
Hervé, Bérénice
...
Gene. 927 (2024) - p. 148734 , 2024
Link:
https://doi.org/10.1016/..
?
3
The clinical value of optical genome mapping in the rapid c..:
Bouassida, Malek
;
Molina‐Gomes, Denise
;
Koraichi, Fairouz
...
Molecular Genetics & Genomic Medicine. 12 (2024) 4 - p. , 2024
Link:
https://doi.org/10.1002/..
?
4
2p25.3 microduplications involving MYT1L: further phenotypi..:
Bouassida, Malek
;
Egloff, Matthieu
;
Levy, Jonathan
...
European Journal of Human Genetics. 31 (2023) 8 - p. 895-904 , 2023
Link:
https://doi.org/10.1038/..
?
5
Evidence for high breakpoint variability in 46, XX, SRY‐pos..:
Capron, Céline
;
Januel, Louis
;
Vieville, Gaëlle
...
Andrology. 10 (2022) 8 - p. 1625-1631 , 2022
Link:
https://doi.org/10.1111/..
?
6
Effects of the implementation of second-line prenatal cell-..:
Duvillier, Clémence
;
Dard, Rodolphe
;
Hervé, Bérénice
...
European Journal of Obstetrics & Gynecology and Reproductive Biology. 267 (2021) - p. 36-41 , 2021
Link:
https://doi.org/10.1016/..
?
7
Terminal 6q deletions cause brain malformations, a phenotyp..:
Lesieur‐Sebellin, Marion
;
Till, Marianne
;
Khau Van Kien, Philippe
...
Prenatal Diagnosis. 42 (2021) 1 - p. 118-135 , 2021
Link:
https://doi.org/10.1002/..
?
8
A high level of tetrasomy 9p mosaicism but no clinical mani..:
Bellil, Hela
;
Herve, Bérenice
;
Herzog, Elodie
...
Journal of Assisted Reproduction and Genetics. 37 (2020) 3 - p. 573-577 , 2020
Link:
https://doi.org/10.1007/..
?
9
Prenatal diagnosis of 2q13 duplications: The crucial role o..:
Bellil, Hela
;
Molina-Gomes, Denise
;
Quibel, Thibaud
...
European Journal of Medical Genetics. 63 (2020) 8 - p. 103956 , 2020
Link:
https://doi.org/10.1016/..
?
10
Chromosomal microarray analysis in fetuses with an isolated..:
Hureaux, Marguerite
;
Guterman, Sarah
;
Hervé, Bérénice
...
Prenatal Diagnosis. 39 (2019) 6 - p. 464-470 , 2019
Link:
https://doi.org/10.1002/..
?
11
Prenatal findings in 1p36 deletion syndrome: New cases and ..:
Guterman, Sarah
;
Beneteau, Claire
;
Redon, Sylvia
...
Prenatal Diagnosis. 39 (2019) 10 - p. 871-882 , 2019
Link:
https://doi.org/10.1002/..
?
12
DNA ligase IV deficiency: Immunoglobulin class deficiency d..:
Dard, Rodolphe
;
Herve, Bérénice
;
Leblanc, Thierry
...
Pediatric Allergy and Immunology. 28 (2017) 3 - p. 298-303 , 2017
Link:
https://doi.org/10.1111/..
?
13
First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleef..:
Guterman, Sarah
;
Hervé, Bérénice
;
Rivière, Julie
...
Journal of Obstetrics and Gynaecology Research. 44 (2017) 3 - p. 570-575 , 2017
Link:
https://doi.org/10.1111/..
?
14
Prevalence of recurrent pathogenic microdeletions and micro..:
Grati, Francesca Romana
;
Molina Gomes, Denise
;
Ferreira, Jose Carlos Pinto B.
...
Prenatal Diagnosis. 35 (2015) 8 - p. 801-809 , 2015
Link:
https://doi.org/10.1002/..
?
15
Are de novo rea(21;21) chromosomes really de novo?:
Hervé, Bérénice
;
Quibel, Thibaud
;
Taieb, Stéphane
...
Clinical Case Reports. 3 (2015) 10 - p. 786-789 , 2015
Link:
https://doi.org/10.1002/..
1-15