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Taşdelen, Elifcan
9  results:
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1

A founder deletion in ECM1 of 1163 bp causes lipoid protein..:

Taşdelen, Elifcan ; Sezer, Abdullah ; An, Isa
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
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2

Novel homozygous frameshift insertion variant in the last e..:

Kablan, Ahmet ; Tasdelen, Elifcan
Italian Journal of Pediatrics.  50 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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3

Novel RETREG1 (FAM134B) founder allele is linked to HSAN2B ..:

Taşdelen, Elifcan ; Calame, Daniel G. ; Akay, Gulsen...
American Journal of Medical Genetics Part A.  188 (2022)  7 - p. 2153-2161 , 2022
Link: https://doi.org/10.1002/..
 
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4

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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5

Skeletal and molecular findings in 51 Cleidocranial dysplas..:

Berkay, Ezgi Gizem ; Elkanova, Leyla ; Kalaycı, Tuğba...
American Journal of Medical Genetics Part A.  185 (2021)  8 - p. 2488-2495 , 2021
Link: https://doi.org/10.1002/..
 
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6

Determination of miR-373 and miR-204 levels in neuronal exo..:

TAŞDELEN, Elifcan ; ÖZEL KIZIL, Erguvan Tuğba ; TEZCAN, Sabiha...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395704/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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7

Skeletal and molecular findings in 51 Cleidocranial dysplas..:

Berkay, Ezgi Gizem ; Elkanova, Leyla ; Kalayci, Tugba...
https://aperta.ulakbim.gov.tr/record/231512.  , 2021
Link: https://aperta.ulakbim.g..
 
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8

Fenotip açıdan Majeed Sendromu olarak değerlendirilen hered..:

Kutay, Nüket ; Taşdelen, Elifcan
Rapor.  , 2020
Link: https://hdl.handle.net/2..
 
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9

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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