Pelin O. Kiper
Ankara, Turkey
Last Updated: 09/26/2026
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Found 8 publications
Two cases with undefined childhood interstitial lung disease: Can it be related to telomere variants?
Journal: Journal of paediatrics and child health
Published: May 20, 2024
Diagnostic yield of microarrays in individuals with non-syndromic developmental delay and intellectual disability.
Journal: Journal of intellectual disability research : JIDR
Published: November 23, 2020
Novel insights into diabetes mellitus due to DNAJC3-defect: Evolution of neurological and endocrine phenotype in the pediatric age group.
Journal: Pediatric diabetes
Published: April 22, 2020
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.
Journal: Journal of child neurology
Published: April 25, 2013
Vesiculopustular eruption in neonatal transient myeloproliferative disorder.
Journal: Indian journal of pediatrics
Published: February 20, 2013
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome.
Journal: American journal of medical genetics. Part A
Published: November 06, 2012
Opinions of Turkish physicians towards termination of pregnancy for fetal disorders.
Journal: Genetic counseling (Geneva, Switzerland)
Published: February 07, 2012
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability.
Journal: Molecular syndromology
Published: September 27, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026