E-LIB Suche - Ergebnisse für: Bousfiha, Amale

1

Impact and prevalence of comorbidities and complications on..:

Djorwé, Soulandi ; Bousfiha, Amale ; Nzoyikorera, Néhémie...
BioMedicine. 14 (2024) 1 - p. , 2024

Link: https://doi.org/10.37796..

2

Evaluation of SARS-CoV-2 infection risks after primary vacc..:

Djorwé, Soulandi ; Bousfiha, Amale ; Nzoyikorera, Néhémie...
BioMedicine. 13 (2023) 3 - p. 31-48 , 2023

Link: https://doi.org/10.37796..

3

Epidemiology, clinical characteristics and risk factors of ..:

Djorwé, Soulandi ; Bousfiha, Amale ; Nzoyikorera, Néhémie...
Access Microbiology. 5 (2023) 4 - p. , 2023

Link: https://doi.org/10.1099/..

4

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/..

5

Chronic myeloid leukemia: cytogenetics and molecular biolog..:

Benchikh, Sara ; Bousfiha, Amale ; El Hamouchi, Adil...
Egyptian Journal of Medical Human Genetics. 23 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

6

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/..

7

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/..

8

Chromosome Abnormalities Related to Reproductive and Sexual..:

Benchikh, Sara ; Bousfiha, Amale ; Razoki, Lunda...
BioMed Research International. 2021 (2021) - p. 1-11 , 2021

Link: https://doi.org/10.1155/..

9

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/..

10

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..

11

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/..

12

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/..

13

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/..

14

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/..

15

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/..