Rana A. Alomar
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 10 publications
Blockchain technology in the pharmaceutical industry: a systematic review.
Journal: PeerJ. Computer science
Published: March 11, 2021
Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans.
Journal: Hepatology (Baltimore, Md.)
Published: April 29, 2019
The many faces of peroxisomal disorders: Lessons from a large Arab cohort.
Journal: Clinical genetics
Published: June 26, 2018
Genomic and phenotypic delineation of congenital microcephaly.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 14, 2018
A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation.
Journal: Genome biology
Published: April 13, 2017
The genetic landscape of familial congenital hydrocephalus.
Journal: Annals of neurology
Published: March 20, 2017
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome.
Journal: American journal of human genetics
Published: February 13, 2017
Identification of a novel MKS locus defined by TMEM107 mutation.
Journal: Human molecular genetics
Published: April 14, 2015
Genomic analysis of primordial dwarfism reveals novel disease genes.
Journal: Genome research
Published: January 07, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026