Recurrent increased nuchal translucency: a first trimester presentation of familial 13p satellite deletion

por Uzun, I, Has, R, Alici, E, Ozdemir, M, Inan, C, Erzincan, S
Publicado 2016

Array-comparative Genomic Hybridization Results in Clinically Affected Cases with Apparently Balanced Chromosomal Rearrangements

por Satkin, NB, Karaman, B, Ergin, S, Kayserili, H, Kalelioglu, IH, Has, R, Yuksel, A, Basaran, S
Publicado 2021