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Search Results - Askander, Omar
Search Results - Askander, Omar
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Homozygous mutation in the ADH6 gene, involved in alcohol metabolism, associated with a multisystem disorder, analogous to the fetal alcohol syndrome
by
Bouhouche, Ahmed
,
Askander, Omar
,
Charoute, Hicham
,
Sabib, Mouna
,
El Quessar, Abdeljalil
,
El Hassani, Amine
,
Erreimi, Naima
Published in
Journal of clinical and translational endocrinology case reports
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Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection
by
Yousfi, Fatima Zahra El
,
Haroun, Abbas Ermilo
,
Nebhani, Chaimae
,
Belayachi, Jihane
,
Askander, Omar
,
Fahime, Elmostafa El
,
Fares, Hakima
,
Ennibi, Khalid
,
Abouqal, Redouane
,
Razine, Rachid
,
Bouhouche, Ahmed
Published in
Archives of virology
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Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome
by
Bouhouche, Ahmed
,
Albaroudi, Nada
,
El Alaoui, My Abdelaziz
,
Askander, Omar
,
Habbadi, Zineb
,
El Hassani, Amine
,
Iraqi, Hinde
,
El Fahime, Elmostafa
,
Belmekki, Mohammed
Published in
Experimental eye research
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Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders
by
Wang, Huilun H
,
Lin, Liangguang L
,
Li, Zexin J
,
Wei, Xiaoqiong
,
Askander, Omar
,
Cappuccio, Gerarda
,
Hashem, Mais O
,
Hubert, Laurence
,
Munnich, Arnold
,
Alqahtani, Mashael
,
Pang, Qi
,
Burmeister, Margit
,
Lu, You
,
Poirier, Karine
,
Besmond, Claude
,
Sun, Shengyi
,
Brunetti-Pierri, Nicola
,
Alkuraya, Fowzan S
,
Qi, Ling
Published in
The Journal of clinical investigation
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Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation
by
Abbassi, Meriame
,
Bourmtane, Abdelhamid
,
Sayel, Hanane
,
EL Mouhi, Hinde
,
Jalte, Meryem
,
Elasri, Yasser Ali
,
Askander, Omar
,
El Fahime, Elmostafa
,
Bouguenouch, Laila
Published in
Molecular biology reports
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A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
by
El Fizazi, Khawla
,
Bouramtane, Abdelhamid
,
Abbassi, Meriame
,
El Asri, Yasser Ali
,
Askander, Omar
,
El Fahime, Mustapha
,
Ouldim, Karim
,
Ridal, Mohammed
,
Bouguenouch, Laila
Published in
American journal of medical genetics. Part A
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Coding-Complete Sequence of a SARS-CoV-2 Strain from an Omicron (B.1.1.529+BA.1) Variant Detected in Morocco
by
Chouati, Taha
,
Hemlali, Mouhssine
,
Melloul, Marouane
,
Alaoui-Amine, Sanaa
,
Rhoulam, Safae
,
Ghamaz, Hamza
,
Ouarab, Maha
,
Askander, Omar
,
Belayachi, Lamiae
,
Touil, Nadia
,
El Mchichi, Bouchra
,
Elannaz, Hicham
,
Laraqui, Abdelillah
,
Elouennass, Mostafa
,
Ennibi, Khalid
,
El Fahime, Elmostafa
Published in
Microbiology resource announcements
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