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Ammar-Khodja, Fatima
89  Ergebnisse:
Personensuche X
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1

ATP6V1B1 recurrent mutations in Algerian deaf patients asso..:

Dahmani, Malika ; Talbi, Sonia ; Ammar-Khodja, Fatima...
International Journal of Pediatric Otorhinolaryngology.  129 (2020)  - p. 109772 , 2020
Link: https://doi.org/10.1016/..
 
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2

Genetic heterogeneity of congenital hearing impairment in A..:

Talbi, Sonia ; Bonnet, Crystel ; Riahi, Zied...
International Journal of Pediatric Otorhinolaryngology.  112 (2018)  - p. 1-5 , 2018
Link: https://doi.org/10.1016/..
 
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3

A novel biallelic splice site mutation of TECTA causes mode..:

Behlouli, Asma ; Bonnet, Crystel ; Abdi, Samia...
International Journal of Pediatric Otorhinolaryngology.  87 (2016)  - p. 28-33 , 2016
Link: https://doi.org/10.1016/..
 
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4

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
Orphanet Journal of Rare Diseases.  10 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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5

Molecular screening of deafness in Algeria: High genetic he..:

Ammar-Khodja, Fatima ; Faugère, Valérie ; Baux, David...
European Journal of Medical Genetics.  52 (2009)  4 - p. 174-179 , 2009
Link: https://doi.org/10.1016/..
 
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6

The spectrum of GJB2 gene mutations in Algerian families wi..:

Talbi, Sonia ; Bonnet, Crystel ; Boudjenah, Farid...
International Journal of Pediatric Otorhinolaryngology.  124 (2019)  - p. 157-160 , 2019
Link: https://doi.org/10.1016/..
 
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7

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0316-8.  , 2015
Link: https://hal.sorbonne-uni..
 
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8

Diversity of the causal genes in hearing impaired Algerian ..:

Ammar-Khodja, Fatima ; Bonnet, Crystel ; Dahmani, Malika...
info:eu-repo/semantics/altIdentifier/doi/10.1002/mgg3.131.  , 2015
Link: https://pasteur.hal.scie..
 
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9

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0316-8.  , 2015
Link: https://hal.sorbonne-uni..
 
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10

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
http://www.ojrd.com/content/10/1/96.  , 2015
Link: http://www.ojrd.com/cont..
 
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11

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0316-8.  , 2015
Link: https://hal.sorbonne-uni..
 
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12

Diversity of the causal genes in hearing impaired Algerian ..:

Ammar-Khodja, Fatima ; Bonnet, Crystel ; Dahmani, Malika...
info:eu-repo/semantics/altIdentifier/doi/10.1002/mgg3.131.  , 2015
Link: https://pasteur.hal.scie..
 
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13

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0316-8.  , 2015
Link: https://hal.sorbonne-uni..
 
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14

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0316-8.  , 2015
Link: https://hal.sorbonne-uni..
 
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15

EPS8L2 is a new causal gene for childhood onset autosomal r..:

Dahmani, Malika ; Ammar-Khodja, Fatima ; Bonnet, Crystel...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13023-015-0316-8.  , 2015
Link: https://hal.sorbonne-uni..
 
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