Kheloud M. Alhamoudi

<scp><i>EMC10</i></scp> homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay

Muhammad Umair, Mariam Ballow, Abdulaziz Asiri et al. · Clinical Genetics · 2020 · 39 citations · Full text

A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia

Kheloud M. Alhamoudi, Javaid Akhter Bhat, Marwan Nashabat et al. · Frontiers in Pediatrics · 2020 · 21 citations · Full text

MTH1 deficiency selectively increases non-cytotoxic oxidative DNA damage in lung cancer cells: more bad news than good?

Hussein H. K. Abbas, Kheloud M. Alhamoudi, Mark D. Evans et al. · BMC Cancer · 2018 · 20 citations · Full text

Mutated <i>RAP1GDS1</i> causes a new syndrome of dysmorphic feature, intellectual disability &amp; speech delay

Abdulaziz Asiri, Essra Aloyouni, Muhammad Umair et al. · Annals of Clinical and Translational Neurology · 2020 · 20 citations · Full text

Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report

Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef et al. · BMC Pulmonary Medicine · 2020 · 19 citations · Full text