Yarali, Oguzhan

Familial Presentation of a Rare <i>NCKAP1 </i>Splice-Site Variant Associated With a Neurodevelopmental Disorder and Cutaneous Manifestations

Diabetes Insipidus as an Early Clinical Indicator of Wolfram Syndrome Type 1: Evidence From a Symptom-Based Screening Approach

Genetic insights and biochemical profiles in hyperlipidemia: a cohort study from Eastern Anatolia

Gene Panel-Based Genotyping of 279 Turkish Maturity-Onset Diabetes of the Young Patients from Eastern Anatolia

Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency

Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency