Mode Al Ojaimi

Genetic Diseases in the UAE

Mode Al Ojaimi, Rabah Almahmoud, Bashar J. Banimortada, Abduljalil Alragheb et autres

ae, kr, lb (code pays fourni par la source)

Molecular and clinical aspects of histone-related disorders

Mode Al Ojaimi, Bashar J. Banimortada, Abduljalil Alragheb, Razan S Hajir et autres

ae, lb (code pays fourni par la source)

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature

Navin B. Ramakrishna, Umar Bin Mohamad Sahari, Yoshikazu Johmura, Nur Ain Ali et autres

sg, jp, sa, de, us, ae, om, lb, tr (code pays fourni par la source)

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature

Navin B. Ramakrishna, Yoshikazu Johmura, Nur Ain Ali, Umar Bin Mohamad Sahari et autres

sg, jp, sa, de, us, ae, om, lb, tr (code pays fourni par la source)

The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population

Tamam Khalaf, Mode Al Ojaimi, Dina Amin Saleh, Alena Sulaiman et autres

es, ae, Égypte, sa, us, kr, gb (code pays fourni par la source)

Author response for "The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population"

Tamam Khalaf, Mode Al Ojaimi, Dina Amin Saleh, Alena Sulaiman et autres

Author response for "The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population"

Tamam Khalaf, Mode Al Ojaimi, Dina Amin Saleh, Alena Sulaiman et autres

Effect of Sleeping Disorders on the Growth Parameters of Lebanese Children

Micheline Katramiz, Antoine Saadé, Mode Al Ojaimi, Mona Nahas Gholmieh

ae, lb (code pays fourni par la source)

Mitochondrial Fission and Fusion: Molecular Mechanisms, Biological Functions, and Related Disorders

Mode Al Ojaimi, Azza Salah, Ayman W. El‐Hattab

ae (code pays fourni par la source)

Disorders of histone methylation: Molecular basis and clinical syndromes

Mode Al Ojaimi, Bashar J. Banimortada, Amna Othman, Korbinian M. Riedhammer et autres

ae, qa, de, sa (code pays fourni par la source)

Comparing the pre–post knowledge score of health-care professionals on a simulation course for COVID-19 PCR sampling

Mode Al Ojaimi, Megan Khairallah, Rania Al Najjar

A homozygous frame‐shift variant in PROSER1 is associated with developmental delay, hypotonia, genitourinary malformations, and distinctive facial features

Azza Salah, Mohammed Almannai, Mode Al Ojaimi, Mandy Radefeldt et autres

ae, us, de (code pays fourni par la source)