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Durmaz, Ceren Damla
37
results:
Search for persons
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Format
Online (37)
Mediatypes
Articles (Online) (27)
Bookchapter (Online) (1)
OpenAccess-fulltext (9)
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english (33)
Sorted by: Relevance
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?
1
Filippi syndrome: Three new families suggest that urinary s..:
Bas, Hasan
;
Durmaz, Ceren Damla
;
Tombak, Merve Celenkoglu
..
American Journal of Medical Genetics Part A. , 2024
Link:
https://doi.org/10.1002/..
?
2
Phenotypic and molecular characterization of five patients ..:
Gökpınar İli, Ezgi
;
Taşdelen, Elifcan
;
Durmaz, Ceren Damla
...
American Journal of Medical Genetics Part A. 188 (2022) 6 - p. 1792-1800 , 2022
Link:
https://doi.org/10.1002/..
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3
MASP1‐related 3MC syndrome in a patient from Turkey:
Durmaz, Ceren Damla
;
Altıner, Şule
American Journal of Medical Genetics Part A. 185 (2021) 7 - p. 2267-2270 , 2021
Link:
https://doi.org/10.1002/..
?
4
Undifferentiated Melanoma Resembling Undifferentiated Round..:
Kavuncuoglu, Altan
;
Durmaz, Ceren Damla
;
Gokoz, Ozay
..
International Journal of Surgical Pathology. 30 (2021) 3 - p. 346-349 , 2021
Link:
https://doi.org/10.1177/..
?
5
Bilateral choanal atresia in an adult woman with pycnodysos..:
Durmaz, Ceren Damla
;
Taş, Vedat
;
Kocaay, Pınar
...
Congenital Anomalies. 57 (2017) 3 - p. 91-92 , 2017
Link:
https://doi.org/10.1111/..
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6
Genetic Analysis of RASD1 as a Candidate Gene for Schizophr..:
Durmaz, Ceren Damla
;
Karabulut, Halil Gürhan
;
Saka, Meram Can
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667215/. , 2022
Link:
http://www.ncbi.nlm.nih...
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7
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypopla..:
Ozbek, Mehmet Nuri
;
Ceylaner, Serdar
;
Demiral, Meliha
...
27d1deb6-22fb-4483-891a-8fde452a756d. , 2020
Link:
https://doi.org/10.4274/..
?
8
Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Id..:
Turgay, Murat
;
USLU YURTERİ, EMİNE
;
AKKAYA, ZEHRA
...
c81beba2-1dae-4b39-930c-bc8062144bfe. , 2019
Link:
https://doi.org/10.1159/..
?
9
A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal C..:
Durmaz, CEREN DAMLA
;
Evans, Gareth
;
Smith, Miriam J
...
8d5bc16f-6528-42d3-b862-71ca55e1236d. , 2018
Link:
https://doi.org/10.1159/..
?
10
Autosomal Recessive Oculodentodigital Dysplasia: A Case Rep..:
Durmaz, CEREN DAMLA
;
KARABULUT, HALİL GÜRHAN
;
Tasdelen, Elifcan
f1b9e40d-4c83-43bd-9273-6117c500383b. , 2018
Link:
https://doi.org/10.1159/..
?
11
WNT Signaling Perturbations Underlie the Genetic Heterogene..:
Beaver, Erin
;
Ellard, Sian
;
Shinawi, Marwan
...
fb9835c2-941a-4e22-b019-04f4695f211c. , 2018
Link:
https://doi.org/10.1016/..
?
12
Şizofreni hastalarında RASD1 geni mutasyonlarının araştırıl..:
Ruhi, Hatice Ilgın
;
Durmaz Özdinç, Ceren Damla
Rapor. , 2020
Link:
https://hdl.handle.net/2..
?
13
Genetic Analysis of RASD1 as a Candidate Gene for Schizophr..:
Ceren Damla Durmaz
;
Halil Gürhan Karabulut
;
Meram Can Saka
...
https://balkanmedicaljournal.org/text.php?lang=en&id=2445. , 2022
Link:
https://doi.org/10.4274/..
?
14
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypopla..:
Meliha Demiral
;
Hüseyin Demirbilek
;
Edip Unal
...
http://www.jcrpe.org/archives/archive-detail/article-preview/ectopic-posterior-pituitary-polydactyly-midfacial-/30877. , 2020
Link:
https://doi.org/10.4274/..
?
15
Two sequential gene expression programs bridged by cell div..:
Sun, Jingjing
;
Durmaz, Ayse Damla
;
Babu, Aswini
..
Development. 151 (2024) 10 - p. , 2024
Link:
https://doi.org/10.1242/..
1-15