Esra Kilic
Ankara, Turkey
Last Updated: 09/26/2026
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Found 11 publications
Meier-Gorlin syndrome type 7: a rare cause of primordial dwarfism: two new cases and literature review.
Journal: Clinical dysmorphology
Published: June 27, 2024
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 31, 2019
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 10, 2018
Preparation of electrospun polyurethane nanofiber mats for the release of doxorubicine.
Journal: Journal of materials science. Materials in medicine
Published: November 01, 2016
A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome.
Journal: Journal of child neurology
Published: October 06, 2015
A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type I.
Journal: American journal of medical genetics. Part A
Published: July 03, 2014
Prenatal diagnosis in a fetus with de-novo 20q11.2q13.1 deletion and review of the literature.
Journal: Clinical dysmorphology
Published: March 27, 2014
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling.
Journal: Human molecular genetics
Published: August 03, 2013
Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): a potential role of pericentrin in hematopoiesis.
Journal: Pediatric blood & cancer
Published: April 24, 2013
Analysis of idiopathic ventricular tachycardia in childhood.
Journal: The Turkish journal of pediatrics
Published: October 26, 2012
Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 gene.
Journal: The Turkish journal of pediatrics
Published: June 28, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026