Aslıhan Kiraz

Erciyes, Turkey

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

Rare X;13 translocation with NR0B1 duplication in partial gonadal dysgenesis: A novel karyotype in DSD cases.

Rare X;13 translocation with NR0B1 duplication in partial gonadal dysgenesis: A novel karyotype in DSD cases.

Journal: Molecular biology reports

Published: August 06, 2025

The Relationship Between Bone Morphogenic Protein-4 and Visceral-Central Adiposity.

The Relationship Between Bone Morphogenic Protein-4 and Visceral-Central Adiposity.

Journal: Pediatric gastroenterology, hepatology & nutrition

Published: October 22, 2024

A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

Journal: American journal of medical genetics. Part A

Published: August 27, 2024

Recurrent symptomatic urolithiasis in a patient with cystic fibrosis.

Recurrent symptomatic urolithiasis in a patient with cystic fibrosis.

Journal: Pediatric nephrology (Berlin, Germany)

Published: March 20, 2024

Are MUC5B and TERT mutations genetic risk factors for pulmonary fibrosis in individuals with severe COVID-19?

Are MUC5B and TERT mutations genetic risk factors for pulmonary fibrosis in individuals with severe COVID-19?

Journal: Tuberkuloz ve toraks

Published: March 13, 2023

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Journal: Journal of medical virology

Published: December 09, 2022

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey.

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey.

Journal: Balkan medical journal

Published: December 03, 2021

A truncating variant in the THOC6 gene with new findings in a patient with Beaulieu-Boycott-Innes syndrome.

A truncating variant in the THOC6 gene with new findings in a patient with Beaulieu-Boycott-Innes syndrome.

Journal: American journal of medical genetics. Part A

Published: October 14, 2021

Restrictive cardiomyopathy with ring chromosome 6 anomaly in a child.

Restrictive cardiomyopathy with ring chromosome 6 anomaly in a child.

Journal: Anatolian journal of cardiology

Published: October 08, 2021

Tubulopathy and hepatomegaly in a 2-year-old boy: Answers.

Tubulopathy and hepatomegaly in a 2-year-old boy: Answers.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 24, 2020

Tubulopathy and hepatomegaly in a 2-year-old boy: Questions.

Tubulopathy and hepatomegaly in a 2-year-old boy: Questions.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 24, 2020

Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C.

Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C.

Journal: The Turkish journal of pediatrics

Published: January 29, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026