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Albuz, Burcu
16
results:
Search for persons
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Format
Online (16)
Mediatypes
Articles (Online) (3)
OpenAccess-fulltext (13)
Languages
english (14)
Sorted by: Relevance
Sorted by: Year
?
1
Evaluating of colchicine use patterns and attack frequency ..:
Akcan, Mehmet Berkay
;
Albuz, Burcu
;
Ozdemir, Ozturk
.
International Journal of Rheumatic Diseases. 26 (2022) 5 - p. 988-991 , 2022
Link:
https://doi.org/10.1111/..
?
2
The high frequency of chromosomal copy number variations an..:
Albuz, Burcu
;
Ozdemir, Ozturk
;
Silan, Fatma
Clinical Neurology and Neurosurgery. 202 (2021) - p. 106487 , 2021
Link:
https://doi.org/10.1016/..
?
3
De novo mutations of the ATP6V1A gene cause developmental e..:
Fassio, Anna
;
Esposito, Alessandro
;
Kato, Mitsuhiro
...
Brain. 141 (2018) 6 - p. 1703-1718 , 2018
Link:
https://doi.org/10.1093/..
?
4
A rare missense Duchenne muscular dystrophy gene variant in..:
Erdoğan, Çağdaş
;
Albuz, Burcu
;
Aydın Demiray
..
The European Research Journal. , 2022
Link:
https://hdl.handle.net/1..
?
5
Analysis of Differences in DNA Damage and Repair Efficacy i..:
Albuz, Burcu
;
Ateşci, Feride Figen
;
Seçme, Mücahit
...
Turk Psikiyatri Dergisi. , 2022
Link:
https://hdl.handle.net/1..
?
6
Jinekolojik kanserlerde yeni nesil dna dizi analizi ile sap..:
Şahin, Hacı Öztürk
;
Karacaer, Kübra Özkan
;
Albuz, Burcu
.
Makale - Uluslararası Hakemli Dergi. , 2020
Link:
http://hdl.handle.net/11..
?
7
Williams-Beuren Sendromlu Çocukların Klinik ve Ekokardiyogr..:
Kayakıran, Eda Didem
;
Albuz, Burcu
;
Çetin, G. Ozan
.
Türkiye Çocuk Hastalıkları Dergisi. , 2020
Link:
https://hdl.handle.net/1..
?
8
A Novel Nonsense Mutation In The EYA1 Gene Found In A Patie..:
Albuz, Burcu
;
Zeybek, Selcan
;
Anlas, Özlem
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
9
Further delineation of ACPHD syndrome and a novel mutation ..:
Öztürk, Menekşe
;
Zeybek, Selcan
;
Farre, G
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
10
Fetus with partial trisomy 4 and t(2;16) due to maternal co..:
Albuz, Burcu
;
Bağcı, Gülseren
;
Özturk, Menekşe
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
11
Co-existence of multiple subclones in ETV6/RUNX1 at diagnos..:
Sen Türk, Nilay
;
Albuz, Burcu
;
Ay, Yılmaz
..
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
12
De novo mutations of the ATP6V1A gene cause developmental e..:
Fassio, Anna
;
Esposito, Alessandro
;
Kato, Mitsuhiro
...
info:eu-repo/semantics/altIdentifier/pmid/29668857. , 2018
Link:
http://hdl.handle.net/11..
?
13
De novo mutations of the ATP6V1A gene cause developmental e..:
Fassio, Anna
;
Esposito, Alessandro
;
Kato, Mitsuhiro
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972584/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
14
Congenital Central Hypothyroidism Caused by a Novel Thyroid..:
Özhan, Bayram
;
Boz, Özlem Anlaş
;
Sarıkepe, Bilge
..
Journal of Clinical Research in Pediatric Endocrinology. , 2017
Link:
https://hdl.handle.net/1..
?
15
Relationship between the DAT1 gene and the effects of methy..:
Kenar, Ayşe Nur İnci
;
Ünal, G.A
;
Güler, H
...
European Review for Medical and Pharmacological Sciences. , 2016
Link:
https://hdl.handle.net/1..
1-15