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Hancer, Veysel Sabri
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Online (73)
Mediatypes
Articles (Online) (30)
OpenAccess-fulltext (43)
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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/..
1-15