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Hervé, Bérénice
125  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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