PB2657: DIFFERENT TYPES OF LEUKEMIAS AND BLEEDING DISORDER DETECTED IN A TURKISH FAMILY WITH GERMLINE RUNX1 MUTATION FOR THE FIRST TIME.

por Ata, Pinar, Demir, Şenol, Arikan, Fatma, Toptas, Tayfur, Arman, Ahmet
Publicado 2023

Novel Growth Hormone-Releasing Hormone Receptor Gene Mutations in Turkish Children with Isolated Growth Hormone Deficiency

por Arman, Ahmet, Dündar, Bumin Nuri, Çetinkaya, Ergun, Erzaim, Nilüfer, Büyükgebiz, Atilla
Publicado 2014

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

por Turan, Serap, Mumm, Steven, Alavanda, Ceren, Kaygusuz, Betul Sare, Gurpinar Tosun, Busra, Arman, Ahmet, Huskey, Margaret, Guran, Tulay, Duan, Shenghui, Bereket, Abdullah, Whyte, Michael P.
Publicado 2022

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

por Arman, Ahmet, Bereket, Abdullah, Coker, Ajda, Kiper, Pelin Özlem Şimşek, Güran, Tülay, Özkan, Behzat, Atay, Zeynep, Akçay, Teoman, Haliloglu, Belma, Boduroglu, Koray, Alanay, Yasemin, Turan, Serap
Publicado 2014