Ola M. Eid

A homozygous mutation in <i>RNU4ATAC</i> as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder

Ghada M. H. Abdel‐Salam, Noriko Miyake, Maha M. Eid et al. · American Journal of Medical Genetics Part A · 2011 · 33 citations

Life Sciences, Genetics, Molecular Genetics +17

Maxillary protraction using orthodontic miniplates in correction of Class III malocclusion during growth

Ola M. Eid, Ahmed Abdel-Fattah Ramadan, Mohamed Nadim · Journal of the World Federation of Orthodontists · 2016 · 16 citations

Dentistry, Maxillofacial Surgery, Orthodontics +15

Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation

Amal M. Mohamed, Hala T. El‐Bassyouni, Asaad El-Gerzawy et al. · Molecular Cytogenetics · 2018 · 15 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

Amal M. Mohamed, Alaa K. Kamel, Maha M. Eid et al. · Molecular Genetics & Genomic Medicine · 2021 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel Mutations in the Displacement Loop of Mitochondrial DNA are Associated with Acute Lymphoblastic Leukemia: A Genetic Sequencing Study

Haitham A. Yacoub, Wael M. Mahmoud, Hatim A. El-Baz et al. · Asian Pacific Journal of Cancer Prevention · 2014 · 11 citations · Full text

Medicine, Genetics, Molecular Genetics +16