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List of works by Namik Kaya

A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.

scientific article

Expanding the mutational landscape and clinical phenotype of the <i>YIF1B</i> related brain disorder

scientific article published on 07 August 2021

First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

scientific article published on 18 May 2019

Identification of novel genomic imbalances in Saudi patients with congenital heart disease.

scientific article published on 25 January 2018

Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy

scientific article published on 31 January 2020

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