Turki M. Sobahy
Jeddah, Saudi Arabia
Last Updated: 09/26/2026
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Found 9 publications
A heterozygous CEBPA mutation disrupting the bZIP domain in a RUNX1 and SRSF2 mutational background causes MDS disease progression.
Journal: Nature communications
Published: August 02, 2023
Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer.
Journal: Ecancermedicalscience
Published: July 17, 2022
Variants of Human Mucin Genes in Clear Cell Renal Cell Carcinoma and their Potential Prognostic and Predictive Values.
Journal: The Gulf journal of oncology
Published: March 31, 2022
Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study.
Journal: Journal of the neurological sciences
Published: July 04, 2021
Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows.
Journal: BMC medical genomics
Published: January 20, 2021
The role of BRCA1/2 in hereditary and familial breast and ovarian cancers.
Journal: Molecular genetics & genomic medicine
Published: February 26, 2019
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 11, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026