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Durmaz, Ceren Damla
37  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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12

Şizofreni hastalarında RASD1 geni mutasyonlarının araştırıl..:

Ruhi, Hatice Ilgın ; Durmaz Özdinç, Ceren Damla
Rapor.  , 2020
Link: https://hdl.handle.net/2..
 
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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/..
 
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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/..
 
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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/..
 
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