Analysis of Xq27.3 Fragility Using the Micronucleus-Fluorescence In situ Hybridization Assay

ανά Özer, Leyla, Ruhi, Hatice Ilgın, Bökesoy, Işık
Τόπος έκδοσης Genome Integr (2020)

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

ανά Kurtulgan, Hande Küçük, Özer, Leyla, Yıldırım, Malik Ejder, Ünsal, Evrim, Aktuna, Süleyman, Baltacı, Volkan, Akkuş, Nejmiye, Sezgin, İlhan
Τόπος έκδοσης Mol Cytogenet (2015)

Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study

ανά Akıncı, Ayşehan, Türkkahraman, Doğa, Tekedereli, İbrahim, Özer, Leyla, Evren, Bahri, Şahin, İbrahim, Kalkan, Tarkan, Çürek, Yusuf, Çamtosun, Emine, Döğer, Esra, Bideci, Aysun, Güven, Ayla, Eren, Erdal, Sangün, Özlem, Çayır, Atilla, Bilir, Pelin, Törel Ergür, Ayça, Ercan, Oya
Τόπος έκδοσης J Clin Res Pediatr Endocrinol (2019)

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

ανά 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
Τόπος έκδοσης Brain (2020)