I. Mendilcioglu

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

G. Luleci, B. Karaman, S. Yakut, 2011, Balkan journal of medical genetics : BJMG.

Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma

G. Luleci, M. Şımşek, S. Yakut, 2014, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Molecular Analysis of Beta-Thalassemia and Sickle Cell Anemia in Antalya

G. Luleci, A. Şanlioğlu, D. Canatan, 2004, Acta Haematologica.

We can Diagnose it if we Consider it. Diagnostic Pitfall for Placenta: Placental Mesenchymal Dysplasia.

S. Yakut, Z. Çetin, I. Mendilcioglu, 2018, Turk patoloji dergisi.

Diagnostic Pitfall for Placenta : Placental Mesenchymal Dysplasia

S. Yakut, Z. Çetin, I. Mendilcioglu, 2018 .

The prenatal diagnosis of familial satellited Yq chromosomes

G. Luleci, M. Şımşek, S. Ozturk, 2011, Turkish Journal of Medical Sciences.

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.

G. Luleci, S. Yakut, Z. Çetin, 2011, Genetic counseling.

PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13).

B. Karaman, S. Yakut, S. Karauzum, 2015, Genetic counseling.

Rare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases / Prenatal Tanıda Nadir Yapısal Kromozom Anomaliler; 10125 Prenatal Olgunun Klinik ve Sitogenetik Bulguları

G. Lüleci, M. Şımşek, S. Yakut, 2015, Turk patoloji dergisi.