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

por Cetin, Z, Mendilcioglu, I, Yakut, S, Berker-Karauzum, S, Karaman, B, Luleci, G
Publicado 2011

Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome

por Yakut, S, Mihci, E, Altiok Clark, O, Cetin, Z, Keser, I, Berker, S, Luleci, G
Publicado 2012

Aplasia Ras Homologous Member I Gene and Development of Glial Tumors

por Yakut, S, Tuncer, MR, Berker, M, Goksu, E, Gurer, I, Ozes, ON, Luleci, G, Karauzum, SB
Publicado 2011

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

por Sanhal, C.Y., Mendilcioglu, I., Ozekinci, M., Yakut, S., Merdun, Z., Simsek, M., Luleci, G.
Publicado 2014

RLIP76 Gene Variants are not Associated with Drug Response in Turkish Epilepsy Patients

por Manguoğlu, E, Akdeniz, S, Dündar, NO, Duman, Ö, Aktekin, B, Haspolat, Ş, Bilge, U, Özel, D, Lüleci, G
Publicado 2011

Short report. The AIDIT and IMPACT conference 2006: Outcomes and future directions

por Doherty, R, Lubinski, J, Manguoglu, E, Luleci, G, Christie, M, Craven, P, Bancroft, E, Mitra, A, Morgan, S, Eeles, R
Publicado 2007