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Molecular Syndromology|April 17, 2023
Fibular Agenesis and Ball-Like Toes Mimicking Preaxial Polydactyly: Prenatal Presentation of Du Pan SyndromeG Tutku Turgut, Ibrahim Halil Kalelioglu, Volkan Karaman, et al.
Acta Cardiologica|February 12, 2013
Cardiovascular abnormalities in Williams syndrome: 20 years'experience in IstanbulYakup Ergul, Kemal Nisli, Hulya Kayserili, et al.
Cytogenetic and Genome Research|July 6, 2021
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual DisabilityTuğba Karaman Mercan, Ozden Altiok Clark, Ozgur Erkal, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 27, 2025
Discovery of novel candidate genes for congenital diaphragmatic hernia via whole exome sequencingG Somayyeh Heidargholizadeh, Gozde Tutku Turgut, Umut Altunoglu, et al.
Cardiology Journal|May 30, 2012
Evaluation of coronary artery abnormalities in Williams syndrome patients using myocardial perfusion scintigraphy and CT angiographyYakup Ergul, Kemal Nisli, Hulya Kayserili, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|September 26, 2018
Follow-Up Studies of cf-DNA Testing from 101 Consecutive Fetuses and Related Ultrasound FindingsSeher Basaran, Recep Has, Ibrahim Halil Kalelioglu, et al.
The Journal of Obstetrics and Gynaecology Research|June 4, 2019
Utilization of neurosonography for evaluation of the corpus callosum malformations in the era of fetal magnetic resonance imagingGurcan Turkyilmaz, Tugba Sarac Sivrikoz, Emircan Erturk, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 2, 2025
Diagnostic contribution of conventional and molecular karyotyping in congenital diaphragmatic hernia related copy number variationsG Somayyeh Heidargholizadeh, Cagri Gulec, Gulnihal Bulut, et al.
European Journal of Medical Genetics|June 10, 2006
The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from TurkeyBirsen Karaman, Melike Aytan, Kader Yilmaz, et al.
European Journal of Medical Genetics|May 23, 2009
Molecular genetic screening of MBS1 locus on chromosome 13 for microdeletions and exclusion of FGF9, GSH1 and CDX2 as causative genes in patients with Moebius syndromeAbdullah Uzumcu, Birsen Karaman, Guven Toksoy, et al.
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