Muhammad Kohailan
4PUBLICATIONS
11CO-AUTHORS
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Publications (4)
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|Jun 13, 2025
Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.Aljazi Al-Maraghi, Rulan Shaath, Katherine Ford
|Oct 25, 2024
A Systematic Review and Comprehensive Analysis of mcr Gene Prevalence in Bacterial Isolates in Arab Countries.Mouayad Zuheir Bakleh, Muhammad Kohailan, Muhammad Marwan
|Jun 22, 2022
A de novo start-loss in EFTUD2 associated with mandibulofacial dysostosis with microcephaly: case report.Muhammad Kohailan, Omayma Al-Saei, Sujitha Padmajeya
|Jun 19, 2022
Patterns and distribution of de novo mutations in multiplex Middle Eastern families.Muhammad Kohailan, Waleed Aamer, Najeeb Syed
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Frequent Collaborators
2 joint publications
Waleed Aamer
2 joint publications
Khalid A Fakhro
1 joint publications
Sasirekha Palaniswamy
1 joint publications
Mouayad Zuheir Bakleh
1 joint publications
Muhammad Marwan
1 joint publications
Abdallah Alhaj Sulaiman
1 joint publications
Katherine Ford
1 joint publications
Jehan AlRayahi
1 joint publications
Elbay Aliyev
1 joint publications
Ruba Benini
