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Ben Ayed, Ikhlas
47
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Online (47)
Mediatypes
Articles (Online) (17)
Bookchapter (Online) (4)
OpenAccess-fulltext (26)
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?
1
Case Report: Pre- and post-natal evolution of Kabuki Syndro..:
Souayeh, Nesrine
;
MARZOUK, Asma
;
Jelalia, Nour
...
F1000Research. 13 (2024) - p. 406 , 2024
Link:
https://doi.org/10.12688..
?
2
Customized targeted massively parallel sequencing enables t..:
Ben Said, Mariem
;
Jallouli, Olfa
;
Ben Aissa, Abir
...
Epilepsia Open. , 2024
Link:
https://doi.org/10.1002/..
?
3
Case report: Functional analysis of the p.Arg507Trp variant..:
Ben Ayed, Ikhlas
;
Jallouli, Olfa
;
Murakami, Yoshiko
...
Frontiers in Neurology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
A new case with the recurrent PURA p.(Phe233del) pathogenic..:
Ben Issa, Abir
;
Ben Ayed, Ikhlas
;
Jallouli, Olfa
...
International Journal of Developmental Neuroscience. 83 (2023) 4 - p. 383-395 , 2023
Link:
https://doi.org/10.1002/..
?
5
Genetic Association of rs1021188 and DNA Methylation Signat..:
Bouzid, Amal
;
Chelly, Ameni
;
Tekari, Adel
...
Frontiers in Medicine. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
6
Evaluation of X chromosome inactivation in endemic Tunisian..:
Abida, Olfa
;
Elloumi, Nesrine
;
Bahloul, Emna
...
Molecular Genetics & Genomic Medicine. 10 (2022) 12 - p. , 2022
Link:
https://doi.org/10.1002/..
?
7
SRD5A3‐CDG: 3D structure modeling, clinical spectrum, and c..:
Ben Ayed, Ikhlas
;
Ouarda, Wael
;
Frikha, Fakher
...
American Journal of Medical Genetics Part A. 185 (2021) 4 - p. 1081-1090 , 2021
Link:
https://doi.org/10.1002/..
?
8
8q21.11 microdeletion syndrome: Delineation of HEY1 as a ca..:
Ben Ayed, Ikhlas
;
Bouzid, Amal
;
Kammoun, Fatma
...
Molecular Genetics & Genomic Medicine. 9 (2021) 11 - p. , 2021
Link:
https://doi.org/10.1002/..
?
9
Further insights into the spectrum phenotype of TRAPPC9 and..:
Ben Ayed, Ikhlas
;
Bouchaala, Wafa
;
Bouzid, Amal
...
European Journal of Medical Genetics. 64 (2021) 12 - p. 104373 , 2021
Link:
https://doi.org/10.1016/..
?
10
Molecular insights into MYO3A kinase domain variants explai..:
Souissi, Amal
;
Abdelmalek Driss, Dorra
;
Chakchouk, Imen
...
Journal of Biomolecular Structure and Dynamics. 40 (2021) 21 - p. 10940-10951 , 2021
Link:
https://doi.org/10.1080/..
?
11
Novel pathogenic mutations and further evidence for clinica..:
Souissi, Amal
;
Ben Said, Mariem
;
Ben Ayed, Ikhlas
...
Journal of Advanced Research. 31 (2021) - p. 13-24 , 2021
Link:
https://doi.org/10.1016/..
?
12
Genetic diagnosis in Sudanese and Tunisian families with sy..:
Yahia, Ashraf
;
Ayed, Ikhlas Ben
;
Hamed, Ahlam A.
...
Annals of Human Genetics. 86 (2022) 4 - p. 181-194 , 2022
Link:
https://doi.org/10.1111/..
?
13
Custom Next‐Generation Sequencing Identifies Novel Mutation..:
Said, Mariem Ben
;
Ayed, Ikhlas Ben
;
Elloumi, Ines
...
Molecular Genetics & Genomic Medicine. 10 (2022) 2 - p. , 2022
Link:
https://doi.org/10.1002/..
?
14
Case report: Functional analysis of the p.Arg507Trp variant..:
Ben Ayed, Ikhlas
;
Jallouli, Olfa
;
Murakami, Yoshiko
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034188/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
15
Evaluation of X chromosome inactivation in endemic Tunisian..:
Abida, Olfa
;
Elloumi, Nesrine
;
Bahloul, Emna
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747557/. , 2022
Link:
http://www.ncbi.nlm.nih...
1-15