Ebru Tuncez

4PUBLICATIONS
18CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesCardiovascular medicine and haematology not elsewhere classifiedPaediatrics not elsewhere classified
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Publications (4)

|Jul 22, 2024
Assessment of Pathogenic Variants in the PAH Gene and Genotype-Phenotype Correlation in Phenylketonuria Patients from Turkey.

Özgür Balasar, Banu Kadıoğlu Yılmaz, Müşerref Başdemirci

|Feb 15, 2023
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies.

Gülay Güleç Ceylan, Esra Habiloğlu, Büşranur Çavdarlı

|Apr 05, 2021
Response to Letter to the Editor: "Atrioventricular canal defect is an infrequent congenital heart disease that can be observed in Bardet-Biedl syndrome".

Evren Gumus, Ebru Tuncez, Ozlem Oz

|Jul 25, 2018
Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficiency Anemia

Fatma Demir Yenigürbüz, Uğur Deveci, Ebru Tuncez

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Frequent Collaborators

1 joint publications

Fatma Demir Yenigürbüz

1 joint publications

Uğur Deveci

1 joint publications

Evren Gumus

1 joint publications

Ozlem Oz