Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

CDH2 and TP53 gene expression in metastatic breast cancer patients

International Eurasian Conference on BioTechnology and BioChemistry (BioTechBioChem 2020), Ankara, Türkiye, 16 - 18 Aralık 2020, ss.20 Sürdürülebilir Kalkınma

CDH2 and TP53 gene expression in metastatic breast cancer patients

International Eurasian Conference on BioTechnology and BioChemistry (BioTechBioChem 2020), Ankara, Türkiye, 16 - 18 Aralık 2020 Sürdürülebilir Kalkınma

SPINK5 Gen Mutasyonu Saptanan Netherton Sendrom'lu Olgu

1. Bursa Uluslararası Katılımlı Genetik Günleri Dermatogenetik Sempozyumu, 09 Ocak 2020

LMNA Gen Mutasyonu Saptanan Nadir Mandibuloakral Displazi Olgusu

1. Bursa Uluslararası Katılımlı Genetik Günleri Dermatogenetik Sempozyumu, 09 Ocak 2020

Schaaf Yang sendromu

4. Ulusal Çocuk Genetik kongresi, İstanbul, Türkiye, 25 - 27 Eylül 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, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.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, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.255-256 identifier

Von Hippel Lindau Patients

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

REVERSE GENETİK İLE TANI KOYULAN NADİR BİR SPASTİK PARAPLEJİ AİLESİ

13.ULUSLARARASI KATILIMLI ULUSAL TIBBİ GENETİK ANABİLİM DALI, Türkiye, 7 - 11 Kasım 2018

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

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.966 Sürdürülebilir Kalkınma identifier

Inversion Y Having Different Phenotypic Expressions at Three Brothers

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.829 identifier

A novel HNF1B mutation in a family with two MODY patients

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.863 identifier

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

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 2017., KOPENHAGEN, Danimarka, 25 - 28 Mayıs 2017

Analysis of The Molecular Markers in 49 AML Patients

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

46 XX SRY pozitif erkek sendromlu olgu

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

Cytogenetic analysis and Y chromosome microdeletion results in infertile males undergoing assisted reproductive technology (ART)

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.302 identifier

Metrikler

Yayın

121

Atıf (WoS)

262

H-İndeks (WoS)

10

Atıf (Scopus)

327

H-İndeks (Scopus)

11

Proje

1

Tez Danışmanlığı

2

Açık Erişim

5
BM Sürdürülebilir Kalkınma Amaçları