Publications by authors named "Randa Alkhalaf"

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Outcomes of cases with elevated 3-hydroxyisovaleryl carnitine report from the newborn screening program.
Fuad Al Mutairi, Randa Alkhalaf, Abdul Rafiq Khan, Ali Al Othaim, Majid Alfadhel

Mol Genet Metab Rep· December 2024

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MEFV c.2230G>T p.(Ala744Ser) rs61732874 previously misclassified as pathogenic variant due to lack of a population specific database.
Lamia Alsubaie, Randa Alkhalaf, Taghrid Aloraini, Manal Amoudi, Abdulrahman Swaid

Ann Hum Genet· September 2020

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Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report.
Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef, Fayhan Alroqi, Alyafee Yusra

BMC Pulm Med· May 2020

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