Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Three novel mutations in 20 patients with hereditary spastic paraparesis.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, cilt.39, sa.9, ss.1551-1557, 2018 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Selection of reliable reference genes for qRT-PCR analysis on head and neck squamous cell carcinomas.

BIOMEDICAL RESEARCH-INDIA, cilt.28, sa.5, ss.2014-2018, 2017 (SCI İndekslerine Giren Dergi) identifier identifier

Altered Plasma MicroRNA Expression in Patients with Mitral Chordae Tendineae Rupture.

The Journal of heart valve disease, cilt.25, ss.580-588, 2016 (SCI Expanded İndekslerine Giren Dergi) identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Y kromozomu mikrodelesyonları ve erkek infertilitesi

Androloji Bülteni, cilt.18, sa.65, ss.126-129, 2016 (Diğer Kurumların Hakemli Dergileri)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Role of Syndecan Gene in the Pathogenesis of Liver Damage in Radioactive Iodine-131 Therapy

32nd Annual Congress of the European-Association-of-Nuclear-Medicine (EANM), Barcelona, İspanya, 12 - 16 Ekim 2019, cilt.46 identifier

A rarely seen 47,XXY/46,XX mosaicism of Klinefelter syndrome: Case report

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.1020 identifier

Ring chromosome 18 in a patient with multiple anomalies

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.960 identifier

The effect of PAI-1 Gene Variants on Development of Thrombophilia in Patients with Klinefelter Syndrome

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.957 identifier

Evaluation of Mutations on Exons 2 and 6 of PTEN Gene in Patients with Gastric Cancer

40th European Human Genetics Conference, Barcelona, İspanya, 31 Mayıs - 01 Haziran 2017, ss.1

Evaluation of certain protein and phosphoprotein expression levels by using western blot technique in head and neck squamous cell carcinoma

41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Türkiye, 3 - 08 Eylül 2016, cilt.283, ss.294 identifier

Evaluation of Activated Signaling Pathways Related to PTEN in Head and Neck Squamose Cell Carcinoma.

10th International Otolaryngology and Head & Neck Surgery Congress., Ankara, Türkiye, 26 - 28 Nisan 2012, ss.1

Investigation of micronucleus frequency in amniotic cells with advanced maternal age

36th FEBS Congress of the Biochemistry for Tomorrows Medicine, Torino, İtalya, 25 - 30 Haziran 2011, cilt.278, ss.247 identifier

A case with Prader-Willi phenotype and a de novo t(2;15)(q31;p11)

39th European Human Genetics Conference, Nice, Fransa, 16 - 19 Haziran 2007, ss.1

Kitap & Kitap Bölümleri

Kalıtsal Hastalıklar ve Moleküler Sitogenetik

Çocuk Genetik Hastalıkları: Mutagenez, Kanserogenez ve Teratogenez - 2020, Mehmet Seven, Editör, Türkiye Klinikleri Yayınevi, Ankara, ss.37-44, 2020 Creative Commons License

Kalıtsal Çocuk Kanserleri ve Kanserogenez

Çocuk Genetik Hastalıkları: Mutagenez, Kanserogenez ve Teratogenez, Mehmet Seven, Editör, Türkiye Klinikleri Yayınevi, Ankara, ss.24-36, 2020 Creative Commons License

Meme Hastalıklarına Klinik Genetik Yaklaşım

MEME HASTALIKLARI KİTABI, Prof. Dr. Zafer Cantürk Prof. Dr. Varol Çelik Prof. Dr. Nilüfer Güler Prof. Dr. Murat Kapkaç Prof. Dr. Ayhan Koyuncu Prof. Dr. Mahmut Müslümano¤lu Prof. Dr. Zafer Utkan, Editör, Güneş Kitabevi, Ankara, ss.1-19, 2012 Creative Commons License