Sevcan Tug Bozdogan

Adana, Turkey

Last Updated: 09/26/2026

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Found 15 publications

Mucolipidosis Type III: A Hidden Challenge in the Differential Diagnosis of Rheumatological Disorders.

Mucolipidosis Type III: A Hidden Challenge in the Differential Diagnosis of Rheumatological Disorders.

Journal: Turkish archives of pediatrics

Published: May 05, 2026

Clinical, demographic and genetic features of pediatric limb-girdle muscular dystrophy in the Çukurova region.

Clinical, demographic and genetic features of pediatric limb-girdle muscular dystrophy in the Çukurova region.

Journal: Italian journal of pediatrics

Published: July 08, 2024

Early diagnostic clues of mucolipidosis type II: Significance of radiological findings.

Early diagnostic clues of mucolipidosis type II: Significance of radiological findings.

Journal: American journal of medical genetics. Part A

Published: July 10, 2023

A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.

A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.

Journal: European journal of breast health

Published: March 29, 2023

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Journal: British journal of haematology

Published: December 09, 2022

Expanding the phenotypic landscape of Gaucher disease type 3c with a novel entity - Transient neonatal cholestasis.

Expanding the phenotypic landscape of Gaucher disease type 3c with a novel entity - Transient neonatal cholestasis.

Journal: European journal of medical genetics

Published: June 30, 2022

WITHDRAWN: Clinical findings and mutational spectrum of neurofibromatosis type 1 patients in a single center of south part of Turkey.

WITHDRAWN: Clinical findings and mutational spectrum of neurofibromatosis type 1 patients in a single center of south part of Turkey.

Journal: Turkish journal of medical sciences

Published: January 31, 2021

A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia.

A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia.

Journal: Journal of pediatric hematology/oncology

Published: September 04, 2020

Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations

Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations

Journal: Journal of clinical research in pediatric endocrinology

Published: July 25, 2020

Evaluation of the results of patients who applied to the Çukurova University, Medical Genetics Department for prenatal diagnosis and determination of genetic counseling principles

Evaluation of the results of patients who applied to the Çukurova University, Medical Genetics Department for prenatal diagnosis and determination of genetic counseling principles

Journal: Turkish journal of medical sciences

Published: April 25, 2020

Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification.

Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification.

Journal: American journal of human genetics

Published: October 09, 2019

BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family history.

BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family history.

Journal: The breast journal

Published: August 08, 2018

Showing 1-12 of 15

Last Updated: 09/26/2026