MediFind found 7 doctor with experience in RUNX1 Familial Platelet Disorder near Turkey. Of these, 7 are Experienced.
Nilgun Tekin practices in Besevler, Turkey. Tekin is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Their top areas of expertise are RUNX1 Familial Platelet Disorder, Diffuse Large B-Cell Lymphoma (DLBCL), Behcet Disease, and Myelodysplastic Syndrome (MDS).
Nuket Kutlay practices in Varlik, Turkey. Kutlay is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Their top areas of expertise are Chromosome 9p Deletion, Chromosome 8p Deletion, Mosaic Trisomy 8, and RUNX1 Familial Platelet Disorder.
Elif Ince practices in Ankara, Turkey. Ms. Ince is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Her top areas of expertise are Chronic Graft Versus Host Disease (cGvHD), Beta Thalassemia, Infantile Neutropenia, Anemia, and Bone Marrow Transplant.
Handan Dincaslan practices in Ankara, Turkey. Dincaslan is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Their top areas of expertise are Retinoblastoma, Osteosarcoma, Adult Soft Tissue Sarcoma, and Medullary Thyroid Carcinoma.
Talia Ileri practices in Ankara, Turkey. Ms. Ileri is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Her top areas of expertise are Thalassemia, Anemia, Beta Thalassemia, Hemoglobinopathy, and Bone Marrow Transplant.
Esra Pekpak practices in Gaziantep, Turkey. Ms. Pekpak is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Her top areas of expertise are Enlarged Liver, Hemophagocytic Lymphohistiocytosis, Factor 7 Deficiency, and Non-Langerhans-Cell Histiocytosis.
Sule Altıner practices in Ankara, Turkey. Ms. Altıner is rated as an Experienced expert by MediFind in the treatment of RUNX1 Familial Platelet Disorder. Her top areas of expertise are Mosaicism, Chromosome 20 Trisomy, Megalencephaly-Capillary Malformation Syndrome, and Chromosome 18p Deletion.
Last Updated: 01/09/2026