Ahmet Kablan

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 5

Top Topics

Intellectual Disability

Dna Methylation

Depressive Symptoms

Top Venues

Italian journal of pediatrics

Twin research and human genetics : the official journal of the International Society for Twin Studies

This page only lists publications with an associated author ORCID identifier.

Publications

Ahmet Kablan, Elifcan Taşdelen
Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature. Italian journal of pediatrics 50 (1) (2024)
Ahmet Kablan, Elifcan Taşdelen
Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature. Italian journal of pediatrics 50 (1) (2024)
Ahmet Kablan, Elifcan Taşdelen
Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature. Italian journal of pediatrics 50 (1) (2024)
Ahmet Kablan, Elifcan Taşdelen
Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature. Italian journal of pediatrics 50 (1) (2024)
Ahmet Kablan, Fatma Sılan, Ozturk Ozdemir
Re-evaluation of Genetic Variants in Parkinson's Disease Using Targeted Panel and Next-Generation Sequencing. Twin research and human genetics : the official journal of the International Society for Twin Studies (2023)