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Bakhchane, Amina
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1

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/..
 
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2

Omenn syndrome caused by a novel homozygous mutation in rec..:

Benhsaien, Ibtihal ; Essadssi, Soukaina ; Elkhattabi, Lamiae...
Immunobiology.  226 (2021)  3 - p. 152090 , 2021
Link: https://doi.org/10.1016/..
 
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3

A Homozygous RAG1 Gene Mutation in a Case of Combined Immun..:

Essadssi, Soukaina ; Benhsaien, Ibtihal ; Bakhchane, Amina...
Human Heredity.  84 (2020)  6 - p. 272-278 , 2020
Link: https://www.jstor.org/st..
 
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4

Further Evidence for the Implication of the MET Gene in Non..:

Bousfiha, Amale ; Riahi, Zied ; Elkhattabi, Lamiae...
Human Heredity.  84 (2019)  3 - p. 109-116 , 2019
Link: https://doi.org/10.1159/..
 
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5

Further Evidence for the Implication of the MET Gene in Non..:

Bousfiha, Amale ; Riahi, Zied ; Elkhattabi, Lamiae...
Human Heredity.  84 (2019)  3 - p. 109-116 , 2019
Link: https://www.jstor.org/st..
 
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6

A Homozygous RAG1 Gene Mutation in a Case of Combined Immun..:

Essadssi, Soukaina ; Benhsaien, Ibtihal ; Bakhchane, Amina...
Human Heredity.  84 (2019)  6 - p. 272-278 , 2019
Link: https://doi.org/10.1159/..
 
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7

Homozygous mutations in PJVK and MYO15A genes associated wi..:

Salime, Sara ; Charif, Majida ; Bousfiha, Amale...
International Journal of Pediatric Otorhinolaryngology.  101 (2017)  - p. 25-29 , 2017
Link: https://doi.org/10.1016/..
 
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8

Novel compound heterozygous mutations in the GPR98 (USH2C) ..:

Bousfiha, Amale ; Bakhchane, Amina ; Charoute, Hicham...
Molecular Biology Reports.  44 (2017)  5 - p. 429-434 , 2017
Link: https://doi.org/10.1007/..
 
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9

A novel PEX1 mutation in a Moroccan family with Zellweger s..:

Bousfiha, Amale ; Bakhchane, Amina ; Charoute, Hicham...
Human Genome Variation.  4 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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10

Novel compound heterozygous MYO7A mutations in Moroccan fam..:

Bakhchane, Amina ; Charif, Majida ; Bousfiha, Amale...
PLOS ONE.  12 (2017)  5 - p. e0176516 , 2017
Link: https://doi.org/10.1371/..
 
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11

Expression faible de A 2chez les donneurs de sang marocains..:

Zarati, Fatima ; Bakhchane, Amina ; Nourlil, Jalal...
Transfusion Clinique et Biologique.  24 (2017)  3 - p. 343 , 2017
Link: https://doi.org/10.1016/..
 
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12

Genetic investigation of XPA gene: high frequency of the c...:

Kindil, Zineb ; Senhaji, Mohamed Amine ; Bakhchane, Amina...
BMC Research Notes.  10 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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13

Expression faible des A2 chez les donneurs de sang marocain..:

Zarati, Fatima ; Bakhchane, Amina ; Nourlil, Jalal...
Transfusion Clinique et Biologique.  23 (2016)  4 - p. 295 , 2016
Link: https://doi.org/10.1016/..
 
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14

Update of the spectrum of GJB2 gene mutations in 152 Morocc..:

Bakhchane, Amina ; Bousfiha, Amale ; Charoute, Hicham...
European Journal of Medical Genetics.  59 (2016)  6-7 - p. 325-329 , 2016
Link: https://doi.org/10.1016/..
 
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15

Novel variants of mitochondrial DNA associated with Type 2 ..:

Charoute, Hicham ; Kefi, Rym ; Bounaceur, Safaa...
Mitochondrial DNA Part A.  29 (2016)  1 - p. 9-13 , 2016
Link: https://doi.org/10.1080/..
 
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