Esra S. Cakar
Ankara, Turkey
Last Updated: 09/26/2026
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Found 9 publications
Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.
Journal: European journal of pediatrics
Published: April 10, 2026
Factors affecting parental decisions for termination of pregnancy in the presence of a prenatal trisomy 21 diagnosis.
Journal: Revista da Associacao Medica Brasileira (1992)
Published: May 10, 2025
Fetal Genetic Diagnosis by Chorionic Villus Sampling: Evaluation of the Five-Year Experience from a Single Center.
Journal: Fetal and pediatric pathology
Published: January 05, 2020
Analysis of cystic hygroma diagnosed in the first trimester: Single-center experience
Journal: Journal of the Turkish German Gynecological Association
Published: July 13, 2019
FOUR CASES OF SIRENOMELIA WITH DIFFERENT MANIFESTATION.
Journal: Genetic counseling (Geneva, Switzerland)
Published: December 03, 2015
Microphthalmia in a case of Edward syndrome.
Journal: Seminars in ophthalmology
Published: January 28, 2014
A retrospective analysis of amniocenteses performed for advanced maternal age and various other indications in Turkish women.
Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Published: October 03, 2012
Association between pre-eclampsia and inherited thrombophilias.
Journal: Fetal and pediatric pathology
Published: September 26, 2012
Role of oxidative stress in preeclampsia and intrauterine growth restriction.
Journal: The journal of obstetrics and gynaecology research
Published: March 03, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026