Yayınlar & Eserler

Diğer Dergilerde Yayınlanan Makaleler

Restriktif dermopatili bir prematüre vaka takdimi

Zeynep Kamil Tıp Bülteni, cilt.40, ss.149-153, 2009 (Diğer Kurumların Hakemli Dergileri)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Von Hippel Lindau Patients

13. BALKAN GENETİK KONGRESİ, Edirne, Türkiye, 16 - 20 Nisan 2019

İKİ LAMİNOPATİ OLGUSU: LMNA GENİ MUTASYONLARI İLE İLİŞKİLİ FENOTİPLER

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Türkiye, 07 Kasım 2018 - 11 Kasım 1918

BBS10 frameshift mutation in a Turkish girl with Bardet Biedl Syndrome.

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 Mayıs 2017

A Novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 Mayıs 2017

Evaluation of BRCA1/BRCA2 test results for Turkish breast cancer families.

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 Mayıs 2017

A novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics 2017., KOPENHAGEN, Danimarka, 25 - 28 Mayıs 2017

BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome

The European Society of Human Genetics 2017, KOPENHAGEN, Danimarka, 25 - 30 Mayıs 2017

Clinical Evaluation of a MDC1A Case Carrying LAMA2 Mutation

ULUSAL TIBBİ GENETİK KONGRESİ, İZMİR ÇEŞME, Türkiye, 5 - 09 Ekim 2016

A novel splice site JAG1 mutation in a Turkish girl with Alagille Syndrome

European Society Of Human Genetics Congress, Barcelona, İspanya, 21 - 24 Mayıs 2016

Analysis of The Molecular Markers in 49 AML Patients

European Society of Human Genetics Congress, Barcelona, İspanya, 21 - 24 Mayıs 2016