Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 3 |
2021 | 1 |
2022 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
A simple and fast spectroscopy-based technique for Covid-19 diagnosis.
Sci Rep. 2021 Aug 18;11(1):16740. doi: 10.1038/s41598-021-95568-5.
Sci Rep. 2021.
PMID: 34408169
Free PMC article.
SARS-CoV-2 Genome Sequence from Morocco, Obtained Using Ion AmpliSeq Technology.
Jouali F, Marchoudi N, El Ansari FZ, Kasmi Y, Chenaoui M, El Aliani A, Azami N, Loukman S, Ennaji MM, Benhida R, Fekkak J.
Jouali F, et al. Among authors: el ansari fz.
Microbiol Resour Announc. 2020 Jul 30;9(31):e00690-20. doi: 10.1128/MRA.00690-20.
Microbiol Resour Announc. 2020.
PMID: 32732235
Free PMC article.
Item in Clipboard
BRCA1/2 variants and copy number alterations status in non familial triple negative breast cancer and high grade serous ovarian cancer.
El Ansari FZ, Jouali F, Fekkak R, Bakkach J, Ghailani Nourouti N, Barakat A, Bennani Mechita M, Fekkak J.
El Ansari FZ, et al.
Hered Cancer Clin Pract. 2022 Aug 19;20(1):29. doi: 10.1186/s13053-022-00236-y.
Hered Cancer Clin Pract. 2022.
PMID: 35986351
Free PMC article.
Item in Clipboard
EGFR, BRCA1, BRCA2 and TP53 genetic profile in Moroccan triple negative breast cancer cases.
Jouali F, El Ansari FZ, Marchoudi N, Barakat A, Zmaimita H, Samlali H, Fekkak J.
Jouali F, et al. Among authors: el ansari fz.
Int J Mol Epidemiol Genet. 2020 Jun 15;11(1):16-25. eCollection 2020.
Int J Mol Epidemiol Genet. 2020.
PMID: 32714499
Free PMC article.
Item in Clipboard
Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC).
El Ansari FZ, Jouali F, Marchoudi N, Bennani MM, Ghailani NN, Barakat A, Fekkak J.
El Ansari FZ, et al.
BMC Cancer. 2020 Aug 10;20(1):747. doi: 10.1186/s12885-020-07250-0.
BMC Cancer. 2020.
PMID: 32778078
Free PMC article.
Item in Clipboard
Cite
Cite