نتائج البحث - Watfa Al‐Mamari
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1
Revisiting the Prevalence of Autism Spectrum Disorder among Omani Children: A multicentre study حسب Watfa Al‐Mamari, Ahmed B. Idris, Samar Dakak, Muna Alshekaili, Zuwaina Al-Harthi, Asia Alnaamani, Fatma Al-Hinai, Saquib Jalees, Moza Al Hatmi, Mohamed El‐Naggari, M. Mazharul Islam
منشور في 2019Artigo -
2
THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder حسب Martin Broly, Bogdan Polevoda, Kamel Awayda, Ning Tong, Jenna M. Lentini, Thomas Besnard, Wallid Deb, Declan O’Rourke, Júlia Baptista, Sian Ellard, Mohammed Almannai, Mais Hashem, Ferdous Abdulwahab, Hanan E. Shamseldin, Saeed M Al-Tala, Fowzan S. Alkuraya, A. S. Leon, Rosa Laura E. van Loon, Alessandra Ferlini, Mariabeatrice Sanchini, Stefania Bigoni, Andrea Ciorba, Hans van Bokhoven, Zafar Iqbal, Almundher Al‐Maawali, Fathiya Al-Murshedi, Anuradha Ganesh, Watfa Al‐Mamari, Sze Chern Lim, Lynn Pais, Natasha J. Brown, Saima Riazuddin, Stéphane Bézieau, Dragony Fu, Bertrand Isidor, Benjamin Cogné, Mitchell R. O’Connell
منشور في 2022Artigo
أدوات البحث:
موضوعات ذات صلة
Acetylation
Allele
Autism
Autism spectrum disorder
Biology
Confidence interval
Environmental health
Gene
Genetics
Intellectual disability
Internal medicine
Loss function
Medicine
Messenger RNA
Missense mutation
Pediatrics
Phenotype
Population
Prevalence
Psychiatry
RNA
Transfer RNA
Translation (biology)