Mohammed A. Aldahmesh
Riyadh, 11211, Saudi Arabia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 43 publications
Genetic investigation of 93 families with microphthalmia or posterior microphthalmos.
Journal: Clinical genetics
Published: November 09, 2017
Congenital glaucoma and CYP1B1: an old story revisited.
Journal: Human genetics
Published: November 07, 2017
Infantile Nephropathic Cystinosis: A Novel CTNS Mutation.
Journal: The Eurasian journal of medicine
Published: June 23, 2017
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract.
Journal: Human genetics
Published: September 06, 2016
Congenital hereditary endothelial dystrophy, not glaucoma, in a child with iris colobomas.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: December 03, 2015
Phenotypes of Recessive Pediatric Cataract in a Cohort of Children with Identified Homozygous Gene Mutations (An American Ophthalmological Society Thesis).
Journal: Transactions of the American Ophthalmological Society
Published: December 02, 2015
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 18, 2015
Clinical Characterization of LRPAP1-Related Pediatric High Myopia.
Journal: Ophthalmology
Published: May 15, 2015
Exome-based case-control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy.
Journal: Human genetics
Published: March 24, 2015
Last Updated: 09/26/2026