Journal articles indexed in SCI, SSCI, and AHCI
7
The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study
JOURNAL OF GYNECOLOGY OBSTETRICS AND HUMAN REPRODUCTION
, vol.48, no.7, pp.521-525, 2019 (SCI-Expanded)



Articles Published in Other Journals
2
Plazminojen aktivatör inhibitör-1 (PAI-1) 4G/4G polimorfizminin gebelik kayıplarıyla ilişkisi
Cumhuriyet Medical Journal
, no.36, pp.350-355, 2014 (Peer-Reviewed Journal)
Papers Presented at Peer-Reviewed Scientific Conferences
25
Family screening of a child with Werdnig-Hoffman’s disease by MLPA
V. Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Turkey, 20 - 22 February 2020, (Summary Text)
Parsiyel Korpus Kallozum Agenezisi, Ventriküler Septal Defekt, Retinoblastom ve Sensorinöral İşitme Kaybı Olan 13q Delesyon Sendromlu Bir Olgu
Türkiye Maternal Fetal Tıp ve Perinatoloji Derneği Ultrasonografi Kursu, Turkey, 31 October - 02 November 2019, (Summary Text)
Parsiyel Korpus Kallozum Agenezisi, Ventriküler Septal Defekt, Retinoblastom ve Sensorinöral İşitme Kaybı Olan 13q Delesyon Sendromlu Bir Olgu
Türkiye Maternal Fetal Tıp ve Perinatoloji Derneği Ultrasonografi Kursu, İstanbul, Turkey, 31 October - 02 November 2019, (Summary Text)
Two diseases associated with chromosome 19 in an infertile male patient
ULUSLARARASI KATILIMLI ERCİYES TIP GENETİK GÜNLERİ, Turkey, 21 - 23 February 2019, (Summary Text)
A rare AMH variant in a case with persistent Mullerian Duct syndrome
ULUSLARARASI KATILIMLI ERCİYES TIP GENETİK GÜNLERİ, Turkey, 21 - 23 February 2019, (Summary Text)
A CASE OF FLOATING-HARBOR SYNDROME WİTH A NOVEL MUTATİON
TBD ULUSLARARASI BİYOKİMYA KONGRESİ 2018 29. ULUSAL BİYOKİMYA KONGRESİ, 26 - 30 October 2018, (Summary Text)
İLİŞKİLİ HASTALIKLARDA HLA-B27 SIKLIĞI
5. SİVAS ROMATOLOJİ GÜNLERİ, Turkey, 15 - 16 September 2018, (Summary Text)
A Familal Case of Hypochondroplasia with Gypsy Origin
erciyes tıp genetik günleri, Turkey, 7 - 10 March 2018, (Summary Text)
A familial case of hypochondroplasia with Gypsy origin
ERCİYES TIP GENETİK GÜNLERİ, Turkey, 7 - 10 March 2018, (Summary Text)
İNMEYLE GELEN PSÖDOKSANTOMA ELASTİKUMLU BİR AİLENİN İNCELENMESİ
53. Ulusal Nöroloji Kongresi, Turkey, 24 - 30 November 2017, (Summary Text)
İnmeyle Gelen Psödoksantoma Elastikumlu Bir Ailenin İncelenmesi
53. Ulusal Nöroloji Kongresi, Antalya, Turkey, 24 - 30 November 2017, (Summary Text)
İNMEYLE GELEN PSÖDOKSANTOMA ELASTİKUM’xxLU BİR AİLENİN İNCELENMESİ
53. ULUSAL NÖROLOJİ KONGRESİ, Turkey, 24 - 30 November 2017, (Summary Text)
Investigation of the levels of malondialdehyde, vitamin E and selenium in patients with Familial Mediterranean Fever
INTERNATIONAL BIOCHEMICALCONGRESS2017, 19 - 23 September 2017, (Summary Text)
investigation of the levels of malondialdehyde, vitamin E and selenium in patients with familial mediterranean fever
international biochemical congress, 19 - 23 September 2017, (Summary Text)
THE PREVALENCE OF FAMILIAL MEDITERRANEAN FEVER (FMF) MUTATIONS IN PEDIATRİC PATIENTS WITH ASTHMA AND ALLERGIC RHINITIS
Erciyes Medical Genetics Days 2017, Kayseri, Turkey, 11 - 13 May 2017, vol.39, pp.56, (Full Text)
The prevalence of familial Mediterranean fever (FMF) mutations in pediatric patients with asthma and allergic rhinitis
Erciyes Tıp Genetik Günleri, Turkey, 11 - 13 May 2017, (Summary Text)
PLAZMINOJEN AKTIVATÖR INHIBITÖR TIP 1 VE ENDOMETRIUMKANSERI ARASINDAKI OLASI ILIŞKI
TBD BİYOKİMYA GÜNLERİ, Sivas, Turkey, 2 - 05 November 2016, (Summary Text)
THE POSSIBLE RELATIONSHIP BETWEEN PLASMINOGENACTIVATOR INHIBITOR TYPE 1 AND ENDOMETRIAL CANCER
TBD biyokimya günleri, Turkey, 2 - 05 November 2016, (Summary Text)

plazminojen aktivatör inhibitör tip 1 ve endometrium kanseri arasındaki olası ilişki
TBD Biyokimya Günleri, Turkey, 2 - 05 November 2016, (Summary Text)

The possible association of some thrombophilic gene polymorphisms with deep vein thrombosis and pulmonary thromboembolism
XII ULUSAL TIBBİ GENETİK KONGRESİ, ÇEŞME/ İZMİR, Turkey, 5 - 09 October 2016, pp.115-120, (Full Text)
Kronik Böbrek Yetmezliği Olgularında Fmf Gen Mefv Ve Saa1 Mutasyonlarının Oranı MutasyonlarınSıklığı Ve Klinik Ve Genetik Zeminde Risk Analizi
10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012, (Summary Text)