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Mkaouar, Rahma
79
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Online (79)
Mediatypes
Articles (Online) (17)
OpenAccess-fulltext (62)
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1
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/..
?
2
Comorbidity of bathing suit ichthyosis and limb-girdle musc..:
Mezzi, Nessrine
;
Zaouak, Anissa
;
Mkaouar, Rahma
...
Gene. 900 (2024) - p. 148127 , 2024
Link:
https://doi.org/10.1016/..
?
3
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/..
?
4
Spectrum of Genetic Diseases in Tunisia: Current Situation ..:
Mezzi, Nessrine
;
Messaoud, Olfa
;
Mkaouar, Rahma
...
Genes. 12 (2021) 11 - p. 1820 , 2021
Link:
https://doi.org/10.3390/..
?
5
Oligogenic Inheritance Underlying Incomplete Penetrance of ..:
Mkaouar, Rahma
;
Abdallah, Lamia Cherif Ben
;
Naouali, Chokri
...
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
6
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/..
?
7
Expanding the clinical phenotype associated with NIPAL4 mut..:
Charfeddine, Cherine
;
Laroussi, Nadia
;
Mkaouar, Rahma
...
PLOS ONE. 16 (2021) 10 - p. e0258777 , 2021
Link:
https://doi.org/10.1371/..
?
8
Congenital lamellar ichthyosis in Tunisia associated with v..:
Zaouak, Anissa
;
Abdessalem, Ghaith
;
Mkaouar, Rahma
...
International Journal of Dermatology. 58 (2019) 7 - p. , 2019
Link:
https://doi.org/10.1111/..
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9
A Tunisian family with a novel mutation in the gene CYP4F22..:
Sayeb, Marwa
;
Riahi, Zied
;
Laroussi, Nadia
...
International Journal of Dermatology. 58 (2019) 12 - p. 1439-1443 , 2019
Link:
https://doi.org/10.1111/..
?
10
Homozygous 2p11.2 deletion supports the implication of ELMO..:
Lahbib, Saida
;
Leblond, Claire S.
;
Hamza, Mariem
...
Journal of Applied Genetics. 60 (2018) 1 - p. 49-56 , 2018
Link:
https://doi.org/10.1007/..
?
11
Spectrum of Genetic Diseases in Tunisia: Current Situation ..:
Mezzi, Nessrine
;
Messaoud, Olfa
;
Mkaouar, Rahma
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes12111820. , 2021
Link:
https://riip.hal.science..
?
12
Alpha-mannosidosis in Tunisian consanguineous families: Pot..:
Mkaouar, Rahma
;
Riahi, Zied
;
Charfeddine, Cherine
...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0258202. , 2021
Link:
https://pasteur.hal.scie..
?
13
Expanding the clinical phenotype associated with NIPAL4 mut..:
Charfeddine, Cherine
;
Laroussi, Nadia
;
Mkaouar, Rahma
...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0258777. , 2021
Link:
https://riip.hal.science..
?
14
Alpha-mannosidosis in Tunisian consanguineous families: Pot..:
Mkaouar, Rahma
;
Riahi, Zied
;
Charfeddine, Cherine
...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0258202. , 2021
Link:
https://pasteur.hal.scie..
?
15
Expanding the clinical phenotype associated with NIPAL4 mut..:
Charfeddine, Cherine
;
Laroussi, Nadia
;
Mkaouar, Rahma
...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0258777. , 2021
Link:
https://hal-riip.archive..
1-15
