Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Articles Published in Other Journals

Restriktif dermopatili bir prematüre vaka takdimi

Zeynep Kamil Tıp Bülteni, vol.40, pp.149-153, 2009 (Other Refereed National Journals)

Refereed Congress / Symposium Publications in Proceedings

Schaaf Yang sendromu

4. Ulusal Çocuk Genetik kongresi, İstanbul, Turkey, 25 - 27 September 2019

FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.893 identifier

A novel intronic ATM gene mutation affecting splicing in a patient with Ataxia-Telangiectasia

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.255-256 identifier

Von Hippel Lindau Patients

13. BALKAN GENETİK KONGRESİ, Edirne, Turkey, 16 - 20 April 2019

İKİ LAMİNOPATİ OLGUSU: LMNA GENİ MUTASYONLARI İLE İLİŞKİLİ FENOTİPLER

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 07 November 2018 - 11 November 1918

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

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

A Novel HNF1B mutation in a family with two MODY patients

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

BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome

The European Society of Human Genetics 2017, KOPENHAGEN, Denmark, 25 - 30 May 2017

A novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics 2017., KOPENHAGEN, Denmark, 25 - 28 May 2017

Silver Russel Sendromlu bir olgu

12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016

Clinical Evaluation of a MDC1A Case Carrying LAMA2 Mutation

ULUSAL TIBBİ GENETİK KONGRESİ, İZMİR ÇEŞME, Turkey, 5 - 09 October 2016

Analysis of The Molecular Markers in 49 AML Patients

European Society of Human Genetics Congress, Barcelona, Spain, 21 - 24 May 2016

46 XX SRY pozitif erkek sendromlu olgu

11. Ulusal Tıbbi Genetik Kongresi, 24-27 Eylül 2014, İstanbul, Turkey, 24 - 27 September 2014

Case presentation The pregnancies of a Down Syndrome mother

6TH EUROPEAN CYTOGENETICS CONFERENCE, 7 - 10 July 2007, vol.15, pp.126

Unusual prenatal case with multiple marker chromosomes

6 TH EUROPEAN CYTOGENETICS CONFERENCE, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.127

A case report with short broad terminal phalanges A new syndrome

ESHG (EUROPEAN SOCIETY OF HUMAN GENETICS), Netherlands, 6 - 09 September 2006, vol.14, pp.156