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Bonnet, Crystel
256
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Online (256)
Mediatypes
Articles (Online) (60)
OpenAccess-fulltext (196)
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1
Genetic variation of TLR3 gene is associated with the outco..:
Soumbara, Tetou
;
Bonnet, Crystel
;
Hamed, Cheikh Tijani
...
BMC Infectious Diseases. 24 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
2
Biallelic variants in TMIE and PDE6B genes mimic Usher synd..:
Abdi, Samia
;
Makrelouf, Mohamed
;
Rous, Issa Nazim
...
Gene Reports. 36 (2024) - p. 101954 , 2024
Link:
https://doi.org/10.1016/..
?
3
Corrigendum: Current phenotypic and genetic spectrum of syn..:
Mkaouar, Rahma
;
Riahi, Zied
;
Marrakchi, Jihene
...
Frontiers in Genetics. 15 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
4
Current phenotypic and genetic spectrum of syndromic deafne..:
Mkaouar, Rahma
;
Riahi, Zied
;
Marrakchi, Jihene
...
Frontiers in Genetics. 15 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
5
Single-cell transcriptomic profiling of the mouse cochlea: ..:
Jean, Philippe
;
Wong Jun Tai, Fabienne
;
Singh-Estivalet, Amrit
...
Proceedings of the National Academy of Sciences. 120 (2023) 26 - p. , 2023
Link:
https://doi.org/10.1073/..
?
6
Deafness: from genetic architecture to gene therapy:
Petit, Christine
;
Bonnet, Crystel
;
Safieddine, Saaïd
Nature Reviews Genetics. 24 (2023) 10 - p. 665-686 , 2023
Link:
https://doi.org/10.1038/..
?
7
Identification a novel pathogenic LRTOMT mutation in Maurit..:
Salame, Malak
;
Bonnet, Crystel
;
Moctar, Ely Cheikh Mohamed
...
European Archives of Oto-Rhino-Laryngology. 280 (2023) 9 - p. 4057-4063 , 2023
Link:
https://doi.org/10.1007/..
?
8
Novel pathogenic WHRN variant causing hearing loss in a mor..:
AitRaise, Imane
;
Amalou, Ghita
;
Redouane, Salaheddine
...
Molecular Biology Reports. 50 (2023) 12 - p. 10663-10669 , 2023
Link:
https://doi.org/10.1007/..
?
9
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Ass..:
AitRaise, Imane
;
Amalou, Ghita
;
Bakhchane, Amina
...
Biochemical Genetics. 62 (2023) 3 - p. 1914-1924 , 2023
Link:
https://doi.org/10.1007/..
?
10
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB v..:
AitRaise, Imane
;
Amalou, Ghita
;
Bousfiha, Amale
...
Molecular Biology Reports. 49 (2022) 5 - p. 3949-3954 , 2022
Link:
https://doi.org/10.1007/..
?
11
Screening of BRCA1/2 variants in Mauritanian breast cancer ..:
Brahim, Selma Mohamed
;
Zein, Ekht Elbenina
;
Bonnet, Crystel
...
BMC Cancer. 22 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
12
Retinal Phenotype of Patients withCLRN1-Associated Usher 3A..:
Smirnov, Vasily M.
;
Nassisi, Marco
;
Mohand-Saïd, Saddek
...
Investigative Opthalmology & Visual Science. 63 (2022) 4 - p. 25 , 2022
Link:
https://doi.org/10.1167/..
?
13
Contributions of Age-Related and Audibility-Related Deficit..:
Varnet, Léo
;
Léger, Agnès C.
;
Boucher, Sophie
...
Frontiers in Aging Neuroscience. 13 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
14
A homozygous MPZL2 deletion is associated with non syndromi..:
Amalou, Ghita
;
Bonnet, Crystel
;
Riahi, Zied
...
International Journal of Pediatric Otorhinolaryngology. 140 (2021) - p. 110481 , 2021
Link:
https://doi.org/10.1016/..
?
15
Alpha-mannosidosis in Tunisian consanguineous families: Pot..:
Mkaouar, Rahma
;
Riahi, Zied
;
Charfeddine, Cherine
...
PLOS ONE. 16 (2021) 10 - p. e0258202 , 2021
Link:
https://doi.org/10.1371/..
1-15