E-LIB Suche - Ergebnisse für: Hancer, Veysel Sabri

1

NOVEL RUNX1 VARIATION IN B-CELL ACUTE LYMPHOBLASTIC LEUKEMI:

Qipa, Egzona ; Acar, Muradiye ; Bozkurt, Sureyya...
Mediterranean Journal of Hematology and Infectious Diseases. 15 (2023) 1 - p. e2023036 , 2023

Link: https://doi.org/10.4084/..

2

A case mimicking chronic myeloid leukemia with t(8;22)(p11;..:

Bayrak, Ayse Gul ; Ucur, Ali ; Daglar Aday, Aynur...
Journal of Hematopathology. 14 (2021) 2 - p. 151-156 , 2021

Link: https://doi.org/10.1007/..

3

INVESTIGATION OF PTGS2, MAGE-A3, CALR, KRT19 AND TMPRSS4 EX..:

Bozkurt, Süreyya ; Yarımcan, Filiz ; Ayhan, Hüseyin...
Genetics & Applications. 4 (2020) 2 - p. 37-42 , 2020

Link: https://doi.org/10.31383..

4

Two Rare Pathogenic HBB Variants in a Patient with β Thalas..:

Hançer, Veysel Sabri ; Fışgın, Tunç ; Büyükdoğan, Murat
Turkish Journal of Hematology. , 2020

Link: https://doi.org/10.4274/..

5

Kruppel-Like Transcription Factor-4 Gene Expression and DNA..:

Coskun, Zeynep Mine ; Ersoz, Melike ; Adas, Mine...
Archives of Medical Research. 50 (2019) 3 - p. 91-97 , 2019

Link: https://doi.org/10.1016/..

6

The Clinical Significance of JAK2V617F Mutation for Philade..:

Hindilerden, Fehmi ; Hindilerden, Ipek Yonal ; Pinarbasi, Binnur...
Clinical Lymphoma Myeloma and Leukemia. 19 (2019) - p. S357 , 2019

Link: https://doi.org/10.1016/..

7

A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with..:

Karacan, İlker ; Diz Küçükkaya, Reyhan ; Karakuş, Fatma Nur...
Turkish Journal of Hematology. 36 (2019) 1 - p. 29-36 , 2019

Link: https://doi.org/10.4274/..

8

A novel ATP6V0A2 mutation causing recessive cutis laxa with..:

Karacan, İlker ; Diz Küçükkaya, Reyhan ; Karakuş, Fatma Nur...
Turkish Journal of Hematology. , 2018

Link: https://doi.org/10.4274/..

9

Three Factor 11 Mutations Associated with Factor XI Deficie..:

Hançer, Veysel Sabri ; Gökgöz, Zafer ; Büyükdoğan, Murat
Turkish Journal of Hematology. 35 (2018) 1 - p. 79-80 , 2018

Link: https://doi.org/10.4274/..

10

β Globin Mutations in Turkish, Northern Iraqi and Albanian ..:

Hancer, Veysel Sabri ; Fisgin, Tunc ; Buyukdogan, Murat..
Thalassemia Reports. 8 (2018) 2 - p. 7286 , 2018

Link: https://doi.org/10.4081/..

11

Three Novel Calreticulin Mutations in Two Turkish Patients:

Hançer, Veysel Sabri ; Tokgöz, Hüseyin ; Güvenç, Serkan..
Turkish Journal of Hematology. 34 (2017) 4 - p. 360-361 , 2017

Link: https://doi.org/10.4274/..

12

The Relationship between P-Selectin Polymorphisms and Throm..:

Alpay, Nilüfer ; Hançer, Veysel Sabri ; Erer, Burak..
Turkish Journal of Hematology. 31 (2014) 4 - p. 357-362 , 2014

Link: https://doi.org/10.4274/..

13

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplas..:

Akpınar, Timur Selçuk ; Hançer, Veysel Sabri ; Nalçacı, Meliha.
Turkish Journal of Hematology. 30 (2013) 1 - p. 8-12 , 2013

Link: https://doi.org/10.4274/..

14

The clinical significance of JAK2V617F mutation for Philade..:

Yonal, Ipek ; Pinarbası, Binnur ; Hindilerden, Fehmi...
Journal of Thrombosis and Thrombolysis. 34 (2012) 3 - p. 388-396 , 2012

Link: https://doi.org/10.1007/..

15

Eculizumab therapy in a child with hemolytic uremic syndrom..:

Caycı, F. Semsa ; Cakar, Nilgun ; Hancer, Veysel Sabri...
Pediatric Nephrology. 27 (2012) 12 - p. 2327-2331 , 2012

Link: https://doi.org/10.1007/..