Kenan Delil
Ihlas Marmara Evleri - I. Kisim, Turkey
Last Updated: 09/26/2026
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Found 15 publications
Hypomagnesemia as a primary clue for the diagnosis of 17q12 deletion syndrome associated with spinal syringomyelia: a case report.
Journal: The Turkish journal of pediatrics
Published: May 01, 2025
Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis.
Journal: The American journal of cardiology
Published: August 27, 2024
Biallelic Mutations in DNAJB11 are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family.
Journal: Molecular syndromology
Published: July 31, 2020
Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report
Journal: Journal of clinical research in pediatric endocrinology
Published: February 06, 2020
Challenges in the treatment of fibrodysplasia ossificans progressiva.
Journal: Rheumatology international
Published: August 04, 2018
Vitamin D receptor gene polymorphisms in children with kidney stone disease.
Journal: The Turkish journal of pediatrics
Published: January 01, 2017
CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33.
Journal: Genetic counseling (Geneva, Switzerland)
Published: February 09, 2016
Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature.
Journal: Journal of clinical research in pediatric endocrinology
Published: January 14, 2016
22q11 deletion syndrome: current perspective.
Journal: The application of clinical genetics
Published: June 10, 2015
Case of fatal heart failure with biventricular noncompaction, genital skeletal abnormalities and mental retardation.
Journal: Anatolian journal of cardiology
Published: January 01, 2015
JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family.
Journal: Journal of clinical immunology
Published: October 13, 2014
Last Updated: 09/26/2026