Original Article

Investigation of APC, MLH1 and MSH2 Mutations in Patients with Hereditary Colorectal Carcinoma: A Single Center Experience
  • Mehmet Buğrahan Düz
Med Bull Haseki 2021; 59: 17-24 DOI: 10.4274/haseki.galenos.2020.6258
Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene
  • Ender Coşkunpınar
  • Ayla Özvarnalı
  • Kıvanç Çefle
  • Ayşe Palanduz
  • Ahmet Gül
  • Derya Öztürk
  • Şükrü Öztürk
  • Şükrü Palanduz
Med Bull Haseki 2018; 56: 42-49 DOI: 10.4274/haseki.42714
Relationship Among Clinical, Laboratory Findings, Disease Severity Scores and Genetic Mutations in Patient with Familial Mediterranean Fever
  • Selda Yavuz
  • Nilgün Selçuk Duru
  • Murat Elevli
Med Bull Haseki 2018; 56: 58-64 DOI: 10.4274/haseki.68077

Case Report

Portal Vein Thrombosis Related to Factor V Leiden Mutation
  • Kerim Çayır
  • Kenan Çadırcı
  • Mehmet Bilici
  • Salim Başol Tekin
  • Mustafa Keleş
  • Habip Emre
Med Bull Haseki 2009; 47: 181-182

Case Report

A Novel Frameshift Mutation in Two Siblings with Merosin-deficient Congenital Muscular Dystrophy
  • Senem Ayça
  • Hamide Betül Gerik Çelebi
  • Sırrı Çam
  • Muzaffer Polat
Med Bull Haseki 2020; 58: 208-210 DOI: 10.4274/haseki.galenos.2019.5177
Early Diagnosis of Fanconi-Bickel Syndrome and a Novel Mutation inSLC2A2 Gene
  • Ezgi Çelikboya
  • Mehmet Şerif Cansever
  • Tanyel Zübarioğlu
  • Gözde Yeşil
  • Nurver Akıncı
Med Bull Haseki 2019; 57: 328-331 DOI: 10.4274/haseki.galenos.2018.4504