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Samri, Imane
20
results:
Search for persons
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Format
Online (20)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (13)
Sorted by: Relevance
Sorted by: Year
?
1
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (T..:
EL Bouchikhi, Ihssane
;
Belhassan, Khadija
;
Moufid, Fatima Zohra
...
Egyptian Journal of Medical Human Genetics. 22 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
2
Molecular and environmental characterization of Noonan synd..:
El Bouchikhi, Ihssane
;
Bouguenouch, Laila
;
Moufid, Fatima Zohra
...
Egyptian Journal of Medical Human Genetics. 21 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
3
Anémie de fanconi au CHU Hassan II Fès: à propos de 6 obser..:
Bouguenouch, Laila
;
Samri, Imane
;
Abbassi, Meryem
...
Pan African Medical Journal. 28 (2017) - p. , 2017
Link:
https://doi.org/10.11604..
?
4
Syndrome de Lynch: à propos d'un cas et revue de la littera..:
Bouguenouch, Laila
;
Samri, Imane
;
Belhassan, Khadija
...
Pan African Medical Journal. 24 (2016) - p. , 2016
Link:
https://doi.org/10.11604..
?
5
Noonan syndrome-causing genes: Molecular update and an asse..:
El Bouchikhi, Ihssane
;
Belhassan, Khadija
;
Moufid, Fatima Zohra
...
International Journal of Pediatrics and Adolescent Medicine. 3 (2016) 4 - p. 133-142 , 2016
Link:
https://doi.org/10.1016/..
?
6
TPMT alleles in the Moroccans:
Janati Idrissi, Meryem
;
Samri, Imane
;
Khabbal, Youssef
..
Clinics and Research in Hepatology and Gastroenterology. 39 (2015) 4 - p. e55-e56 , 2015
Link:
https://doi.org/10.1016/..
?
7
Marqueurs chromosomiques: à propos d'un cas:
Samri, Imane
;
Bouguenouch, Laila
;
Hamdaoui, Hasna
...
Pan African Medical Journal. 15 (2013) - p. , 2013
Link:
https://doi.org/10.11604..
?
8
Absence of GATA4 Mutations in Moroccan Patients with Atrial..:
El Bouchikhi, Ihssane
;
Bouguenouch, Laila
;
Moufid, Fatima Zohra
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7651766/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
9
GATA4 molecular screening and assessment of environmental r..:
EL Bouchikhi, Ihssane
;
Belhassan, Khadija
;
Moufid, Fatima Zohra
...
https://www.ajol.info/index.php/ahs/article/view/180224/169570. , 2018
Link:
https://www.ajol.info/in..
?
10
NKX2-5 molecular screening and assessment of variant rate a..:
Bouchikhi, Ihssane El
;
Bouguenouch, Laila
;
Moufid, Fatima Zohra
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864982/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
11
Noonan syndrome-causing genes: Molecular update and an asse..:
El Bouchikhi, Ihssane
;
Belhassan, Khadija
;
Moufid, Fatima Zohra
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372459/. , 2016
Link:
http://www.ncbi.nlm.nih...
?
12
Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (T..:
Ihssane EL Bouchikhi
;
Khadija Belhassan
;
Fatima Zohra Moufid
...
https://doi.org/10.1186/s43042-021-00136-1. , 2021
Link:
https://doi.org/10.1186/..
?
13
Molecular and environmental characterization of Noonan synd..:
Ihssane El Bouchikhi
;
Laila Bouguenouch
;
Fatima Zohra Moufid
...
http://link.springer.com/article/10.1186/s43042-020-0047-9. , 2020
Link:
https://doi.org/10.1186/..
?
14
Absence of GATA4 Mutations in Moroccan Patients with Atrial..:
Ihssane El Bouchikhi
;
Laila Bouguenouch
;
Fatima Zohra Moufid
...
https://eajm.org/en/absence-of-gata4-mutations-in-moroccan-patients-with-atrial-septal-defect-asd-provides-further-evidence-of-limited-involvement-of-gata4-in-major-congenital-heart-defects-133296. , 2020
Link:
https://doi.org/10.5152/..
?
15
Anémie de fanconi au CHU Hassan II Fès: à propos de 6 obser..:
Laila Bouguenouch
;
Imane Samri
;
Meryem Abbassi
...
https://www.panafrican-med-journal.com/content/article/28/286/pdf/286.pdf. , 2017
Link:
https://doi.org/10.11604..
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