An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation

por Kutukculer, Necil, Karaca, Neslihan Edeer, Aksu, Guzide, Aykut, Ayca, Pariltay, Erhan, Cogulu, Ozgur
Publicado 2018

DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo

por Bolat, Hilmi, Ercan, Eyüp S., Ünsel-Bolat, Gül, Tahillioğlu, Akin, Yazici, Kemal U., Bacanli, Ali, Pariltay, Erhan, Aygüneş Jafari, Duygu, Kosova, Buket, Özgül, Semiha, Rohde, Luis A., Akin, Haluk
Publicado 2020

20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey

por DURMAZ, Burak, BOLAT, Hilmi, CENGİSİZ, Zehra, AKERCAN, Fuat, SÖZEN TÜRK, Tuba, PARILTAY, Erhan, SOLMAZ, Aslı Ece, KAZANDI, Mert, KARACA, Emin, DURMAZ, Asude, AYKUT, Ayça, SAĞOL, Sermet, AKIN, Haluk, ÖZKINAY, Ferda, ÇOĞULU, Özgür
Publicado 2021