Hassan Rouba-El Hamouchi
1 Place Louis Pasteur
Casablanca, 20360, Morocco
Casablanca, 20360, Morocco
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.
Journal: Molecular biology reports
Published: August 23, 2021
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome.
Journal: International journal of pediatric otorhinolaryngology
Published: March 29, 2018
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.
Journal: Gene
Published: January 01, 2018
Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.
Journal: Molecular biology reports
Published: May 19, 2016
Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.
Journal: European journal of medical genetics
Published: December 15, 2015
Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco.
Journal: BMC urology
Published: April 30, 2015
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
Journal: Gene
Published: March 12, 2015
Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.
Journal: Lipids in health and disease
Published: December 24, 2013
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.
Journal: Archives of dermatological research
Published: August 25, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026