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Albuz, Burcu
16  results:
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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/..
 
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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/..
 
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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/..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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...
 
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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..
 
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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..
 
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