An Incidental Detection of a Cryptic Complex Chromosome Rearrangement Found During NGS Based PGT-SR: A Case Report

por Özer, Leyla, Aktuna, Suleyman, Unsal, Evrim, Baltaci, Aysun, Baltaci, Volkan
Publicado 2022

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

por Kurtulgan, Hande Küçük, Özer, Leyla, Yıldırım, Malik Ejder, Ünsal, Evrim, Aktuna, Süleyman, Baltacı, Volkan, Akkuş, Nejmiye, Sezgin, İlhan
Publicado 2015

Oocyte maturation abnormalities - A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina

por Hatırnaz, Şafak, Saynur Hatırnaz, Ebru, Ellibeş Kaya, Aşkı, Hatırnaz, Kaan, Soyer Çalışkan, Canan, Sezer, Özlem, Dokuzeylül Güngor, Nur, Demirel, Cem, Baltacı, Volkan, Tan, Seang, Dahan, Michael
Publicado 2022

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

por Neuray, Caroline, Maroofian, Reza, Scala, Marcello, Sultan, Tipu, Pai, Gurpur S, Mojarrad, Majid, Khashab, Heba El, deHoll, Leigh, Yue, Wyatt, Alsaif, Hessa S, Zanetti, Maria N, Bello, Oscar, Person, Richard, Eslahi, Atieh, Khazaei, Zaynab, Feizabadi, Masoumeh H, Efthymiou, Stephanie, El-Bassyouni, Hala T, Soliman, Doaa R, Tekes, Selahattin, Ozer, Leyla, Baltaci, Volkan, Khan, Suliman, Beetz, Christian, Amr, Khalda S, Salpietro, Vincenzo, Jamshidi, Yalda, Alkuraya, Fowzan S, Houlden, Henry
Publicado 2020