Ali M. Hellani
Khobar, Saudi Arabia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: January 29, 2016
Clinical and molecular characterization of maturity onset-diabetes of the young caused by hepatocyte nuclear factor-4 alpha mutation: red flags for prediction of the diagnosis.
Journal: Annals of Saudi medicine
Published: October 01, 2014
Neurologic injury in isolated sulfite oxidase deficiency.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: January 04, 2014
Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome.
Journal: Ophthalmic genetics
Published: September 05, 2013
Partial duplication of chromosome 19 associated with syndromic duane retraction syndrome.
Journal: Ophthalmic genetics
Published: August 20, 2013
Ophthalmologic observations in a patient with partial mosaic trisomy 8.
Journal: Ophthalmic genetics
Published: February 15, 2013
Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: December 20, 2012
Successful pregnancies after combined human leukocyte antigen direct genotyping and preimplantation genetic diagnosis utilizing multiple displacement amplification.
Journal: Saudi medical journal
Published: October 11, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026