Sarenur B. Yilmaz
Dr. Sare Nur Yilmaz
Istanbul, 34758, Turkey
Istanbul, 34758, Turkey
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
Expanding the Clinical and Molecular Spectrum of TUBB2B Through Distinct Variants Identified Across Multiple Families.
Journal: medRxiv : the preprint server for health sciences
Published: January 08, 2026
Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis.
Journal: Ophthalmic genetics
Published: March 14, 2024
Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.
Journal: American journal of human genetics
Published: May 03, 2019
Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome.
Journal: Annals of dermatology
Published: May 09, 2018
Ear atresia: Is there a role of apoptosis-regulating miRNAs?
Journal: Northern clinics of Istanbul
Published: August 02, 2017
Cilioretinal artery: Vasculogenesis might be promoted by plasminogen activator inhibitor-1 5G allele.
Journal: Ophthalmic genetics
Published: February 02, 2017
Laparoscopic cholecystectomy in an adult with agenesis of right hemidiaphragm and limb reduction defects: First report in literature.
Journal: Northern clinics of Istanbul
Published: July 05, 2015
Lentiginoses in polycythemia vera patient: Is there a role for JAK2 (V617F) mutation?
Journal: JAK-STAT
Published: March 06, 2015
Relation of stem cell markers ALDH1 and CD44 with clinicopathological factors in urothelial carcinomas of urinary bladder.
Journal: International journal of clinical and experimental medicine
Published: January 11, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026