Ebru Tuncez (Ebru Tunçez)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 9

Top Topics

Peritoneal Dialysis

Systematic Review

Congenital Heart Disease

Ejection Fraction

Top Venues

Revista da Associacao Medica Brasileira (1992)

Biochemical genetics

Turkish journal of haematology : official journal of Turkish Society of Haematology

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Özgür Balasar, Banu Kadıoğlu Yılmaz, Muserref Basdemirci, Hatice Koçak Eker, Büşra Eser Çavdartepe, Levent Şimşek, Ebru Tuncez, Fahrettin Duymuş
Assessment of Pathogenic Variants in the PAH Gene and Genotype-Phenotype Correlation in Phenylketonuria Patients from Turkey. Biochemical genetics (2024)
Gülay Güleç Ceylan, Esra Habiloğlu, Busranur Erozan Cavdarli, Ebru Tuncez, Sule Bilen, Özlem Yayıcı Köken, C Nur Semerci Gündüz
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992) 69 (2) (2023)
Gülay Güleç Ceylan, Esra Habiloğlu, Busranur Erozan Cavdarli, Ebru Tuncez, Sule Bilen, Özlem Yayıcı Köken, C Nur Semerci Gündüz
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992) 69 (2) (2023)
Gülay Güleç Ceylan, Esra Habiloğlu, Busranur Erozan Cavdarli, Ebru Tuncez, Sule Bilen, Özlem Yayıcı Köken, C Nur Semerci Gündüz
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992) (2023)
Gülay Güleç Ceylan, Esra Habiloğlu, Busranur Erozan Cavdarli, Ebru Tuncez, Sule Bilen, Özlem Yayıcı Köken, C Nur Semerci Gündüz
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992) (2023)
Gülay Güleç Ceylan, Esra Habiloğlu, Busranur Erozan Cavdarli, Ebru Tuncez, Sule Bilen, Özlem Yayıcı Köken, C Nur Semerci Gündüz
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992) (2023)
Gülay Güleç Ceylan, Esra Habiloğlu, Busranur Erozan Cavdarli, Ebru Tuncez, Sule Bilen, Özlem Yayıcı Köken, C Nur Semerci Gündüz
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies. Revista da Associacao Medica Brasileira (1992) (2023)
Evren Gumus, Ebru Tuncez, Ozlem Oz, Merve Saka Güvenç
Response to Letter to the Editor: "Atrioventricular canal defect is an infrequent congenital heart disease that can be observed in Bardet-Biedl syndrome". Annals of human genetics 85 (3-4) (2021)
Fatma Demir Yenigürbüz, Uğur Deveci, Ebru Tuncez
Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficiency Anemia Turkish journal of haematology : official journal of Turkish Society of Haematology 36 (1) (2018)