SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.351, 2022 (SCI-Expanded)
Investigation of Genes Associated with Multiple Pituitary Hormone Deficiencies <i>via</i> Next Generation Sequencing Technology
HORMONE RESEARCH IN PAEDIATRICS
, sa.SUPPL 2, ss.91-92, 2022 (SCI-Expanded)
Evaluation of Early Puberty in Patients with MC2R Deficiency
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.354, 2022 (SCI-Expanded)
Evaluation of Genetic Etiology in Children Born Small for Gestational Age with Persistent Short Stature: Preliminary Results
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.313, 2022 (SCI-Expanded)
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.
Journal of clinical research in pediatric endocrinology
, cilt.14, sa.2, ss.153-171, 2022 (SCI-Expanded)
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
, cilt.14, sa.2, ss.153-171, 2022 (SCI-Expanded)
Sequence of MKRN3 and DLK1 genes in cases with familial central precocious puberty
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.167-168, 2021 (SCI-Expanded)
Two cases with central precocious puberty caused by paternally inherited novel variants in DLK1gene
EUROPEAN JOURNAL OF HUMAN GENETICS
, sa.SUPPL 1, ss.213, 2020 (SCI-Expanded)
Idiopathic angioedema with F12 mutation: is it a new entity?
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
, cilt.114, sa.2, ss.154-6, 2015 (SCI-Expanded)
Novel NLRP7 mutations in familial recurrent hydatidiform mole: are NLRP7 mutations a risk for recurrent reproductive wastage?
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY
, cilt.170, sa.1, ss.188-192, 2013 (SCI-Expanded)
Diğer Dergilerde Yayınlanan Makaleler
JAG1 MUTATION SPECTRUM IN CASES WITH ALAGILLE SYNDROME FROM TURKIYE
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
, cilt.86, sa.4, ss.327-335, 2023 (ESCI)
CLINICAL AND MOLECULAR RESULTS OF SIX CASES WITH ROBERTS SYNDROME: REVIEW OF CASES FROM TURKIYE
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
, cilt.85, sa.4, ss.501-510, 2022 (Scopus)
SENDROMİK VE NON-SENDROMİK KRANİYOSİNOSTOZ OLGULARINDA FGFR1-3, TWIST1, MSX2, POR, FREM1 VE RAB23 GENLERİNİN MOLEKÜLER ANALİZİ
İSTANBUL TIP FAKÜLTESİ DERGİSİ
, cilt.82, sa.2, ss.9-10, 2019 (Hakemli Dergi)
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
Gebelik Haftasına Göre Küçük Doğan (Sga) Çocuklarda Sebat Eden Boy Kısalığının Etiyolojisinin Genetik Analizler Ile Değerlendirilmesi
15.ULUSLARARASI KATILIMLI, ULUSAL TIBBİ GENETİK KONGRESİ, Muğla, Türkiye, 9 - 13 Kasım 2022, ss.189
Çoğul Hipofiz Hormon Eksikliklerinde İlişkili Genlerin Yeni Nesil Dizileme Teknolojisi İle Araştırılması
XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 06 Ekim 2021
Ailevi Erken Puberte Olgularında MKRN3 ve DLK1 Genlerinin Dizilenmesi
XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrimiçi Kongresi , 30 Ekim - 01 Kasım 2020, ss.12
S-29 - Spectrum of Skeletal Abnormalities and Pathogenic RUNX2 Variants in 50 CleidocranialPatients from Turkey
13TH BALKAN CONGRESS OF HUMAN GENETICS, 17 - 20 Nisan 2019
Tip III Herediter Anjiödem Hastalarının Klinik ve Genetik Özelliklerinin Analizi
XX. Ulusal Allerji ve Klinik immunoloji Kongresi, Antalya, Türkiye, 2 - 06 Kasım 2013, ss.51
Molecular Test Results of Syndromic Craniosynostosis Patients:genotype-phenotype correlations
European Human Genetic Congress, Fransa, 1 - 04 Haziran 2013, ss.99