Prenatal diagnosis of a de novo partial trisomy 6q and partial monosomy 18p associated with cephalocele: A case report
Karaman, A, Karaman, B, Çetinkaya, A, Karaman, S, Demirci, O
Array-comparative genomic hybridization results in clinically affected cases with apparently balanced chromosomal rearrangements
Satkin, NB, Karaman, B, Ergin, S, Kayserili, H, Kalelioglu, IH, Has, R, Yuksel, A, Basaran, S
Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
Cetin, Z, Mendilcioglu, I, Yakut, S, Berker-Karauzum, S, Karaman, B, Luleci, G