SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Induction of apoptosis by metformin and progesterone in estrogen-induced endometrial hyperplasia in rats: involvement of the bcl-2 family proteins.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, cilt.34, ss.433-436, 2018 (SCI Expanded İndekslerine Giren Dergi)
NF1 gene variant allele frequencies comparison of Turkish population with databases
Journal Of Biotechnology, 2017 (SCI İndekslerine Giren Dergi)
Ten cases with 46,XX testicular disorder of sex development: single center experience.
International braz j urol : official journal of the Brazilian Society of Urology, cilt.43, ss.770-775, 2017 (SCI Expanded İndekslerine Giren Dergi)
THE EXPRESSION LEVEL OF BRMS1 IN COLON CANCER PATIENTS AND ITS CLINICAL SIGNIFICANCE
CIENCIA E TECNICA VITIVINICOLA, cilt.30, ss.148-155, 2015 (SCI Expanded İndekslerine Giren Dergi)
Is TNF-alpha gene polymorphism related to pulmonary functions and prognosis as determined by FEV1, BMI, COPD exacerbation and hospitalization in patients with smoking-related COPD in a Turkish population?
REVISTA PORTUGUESA DE PNEUMOLOGIA, cilt.20, ss.305-310, 2014 (SCI İndekslerine Giren Dergi)
Özet
AN UNCOMMON CAUSE OF INFERTILITY: Y;1 TRANSLOCATION AND PGD TRIAL
GENETIC COUNSELING, cilt.25, ss.353-355, 2014 (SCI İndekslerine Giren Dergi)
PARTIAL TRISOMY 3q IN A CHILD WITH SACROCOCCYGEAL TERATOMA AND CORNELIA DE LANGE SYNDROME PHENOTYPE
GENETIC COUNSELING, cilt.22, ss.199-205, 2011 (SCI İndekslerine Giren Dergi)
Özet
Expression of WT1 gene in multiple myeloma patients at diagnosis: is WT1 gene expression a useful marker in multiple myeloma?
HEMATOLOGY, cilt.15, ss.39-42, 2010 (SCI İndekslerine Giren Dergi)
Özet
A UNIQUE CASE OF A PATIENT WITH PARTIAL TRISOMY 22 AND LIPODYSTROPHY: IS IT A NEW SYNDROME DUE TO AN IGF-IR MUTATION?
GENETIC COUNSELING, cilt.21, ss.187-197, 2010 (SCI İndekslerine Giren Dergi)
Özet
A CASE WITH A RARE CHROMOSOMAL ABNORMALITY: ISOCHROMOSOME 18p
GENETIC COUNSELING, cilt.21, ss.69-74, 2010 (SCI İndekslerine Giren Dergi)
Özet
Frank-ter Haar syndrome with unusual clinical features
EUROPEAN JOURNAL OF MEDICAL GENETICS, cilt.52, ss.247-249, 2009 (SCI İndekslerine Giren Dergi)
Özet
Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users
CANCER EPIDEMIOLOGY, cilt.33, ss.47-50, 2009 (SCI İndekslerine Giren Dergi)
Özet
FLUORESCENCE IN SITU HYBRIDIZATION AND SINGLE NUCLEOTIDE POLYMORPHISM OF A NEW CASE WITH INV DUP DEL(8p)
GENETIC COUNSELING, cilt.20, ss.333-340, 2009 (SCI İndekslerine Giren Dergi)
Özet
Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)
INDIAN JOURNAL OF MEDICAL RESEARCH, cilt.128, ss.666-668, 2008 (SCI İndekslerine Giren Dergi)
CAN THE CLASSICAL EUCHROMATIC VARIANTS OF 9q12/qh+ CAUSE RECURRENT ABORTIONS?
GENETIC COUNSELING, cilt.19, ss.281-286, 2008 (SCI İndekslerine Giren Dergi)
Özet
The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, cilt.71, ss.396-404, 2008 (SCI İndekslerine Giren Dergi)
Özet
Prenatal Diagnosis of Unique Translocation t (7;15)(q11. 23;q26. 3) in a Fetus.
Egyptian Journal of Medical Human Genetics, ss.105-110, 2007 (SCI Expanded İndekslerine Giren Dergi)
Triple-X syndrome accompanied by congenital adrenal hyperplasia: case report
TURKISH JOURNAL OF PEDIATRICS, cilt.46, ss.377-379, 2004 (SCI İndekslerine Giren Dergi)
Özet
A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype
ANNALES DE GENETIQUE, cilt.45, ss.181-183, 2002 (SCI İndekslerine Giren Dergi)
Özet
A case with Waardenburg syndrome presenting with two separate translocations - one reciprocal and one complex
CLINICAL DYSMORPHOLOGY, cilt.10, ss.65-66, 2001 (SCI İndekslerine Giren Dergi)
Özet
A case with two separate complex translocations 46,XY,t(1;8)(q32.3;q24.1), t(4;7)->(7ter -> p13 :: 7q34 -> q31.2 :: 4p15.2 -> qter), (7qter -> q34 :: 7p13 -> q31.2 :: 4p15.2 -> pter)
CYTOGENETICS AND CELL GENETICS, ss.159, 1999 (SCI Expanded İndekslerine Giren Dergi)
Do non-steroidal anti-inflammatory drugs induce sister chromatid exchanges in T lymphocytes?
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, cilt.24, ss.84-87, 1996 (SCI İndekslerine Giren Dergi)
Özet
SISTER-CHROMATID EXCHANGE INDUCING EFFECT OF SMOKELESS TOBACCO USING ON T-LYMPHOCYTE CHROMOSOMES
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS, cilt.334, ss.209-212, 1995 (SCI İndekslerine Giren Dergi)
Özet
Diğer Dergilerde Yayınlanan Makaleler
Tümör Nekrosis Faktör-? -308(A/G) Gen Polimorfizminin Behçet Hastalığının Aktif ve İnaktif Fazlarında Araştırılması
SAĞLIK BİLİMLERİ DERGİSİ, cilt.21, ss.75-81, 2012 (Hakemli Üniversite Dergisi)
Prothrombin, factor-V Leiden, and plasminogen activator ınhibitor type 1 gene polymorphisms in hemodialysis patients with/without arteriovenous fistula thrombosis
Nephro-Urology Monthly, cilt.2, ss.314-319, 2010 (Hakemli Üniversite Dergisi)
İnvazif Prenatal Tanı Yöntemleri Uygulanan 2295 Olgunun Retrospektif Analizi
PERİNATOLOJİ DERGİSİ, ss.116-119, 2008 (Hakemli Üniversite Dergisi)
Amenoreli Hastaların Sitogenetik Analiz Sonuçlarının Değerlendirilmesi
Türkiye Klinikleri Dergisi, ss.83-87, 2008 (Hakemli Üniversite Dergisi)
A case of partial trisomy 13 with features similar to ‘C’ Syndrome. Bulguları C sendromuna benzeyen parsiyel trizomi
ERCİYES TIP DERGİSİ, ss.159-163, 2007 (Hakemli Üniversite Dergisi)
Arteriyo-Venöz Fistül Trombozu Gelişen Ve Gelişmeyen Kronik Böbrek Yetmezliği Olan Hastalarda Metilentetrahidrofolat Redüktaz Polimorfizmlerinin Araştırılması.
Erciyes Üniversitesi Sağlık Bilimleri Dergisi, cilt.16, ss.121-128, 2007 (Hakemli Üniversite Dergisi)
Frequency of the common G985A mutation in the medium-chain acyl-coa dehydrogenase gene in Turkish population
SAĞLIK BİLİMLERİ DERGİSİ, cilt.29, ss.263-267, 2007 (Hakemli Üniversite Dergisi)
Gastrointestinal sistem kanserlerinde Metilentetrahidrofolat Redüktaz Geni 677C/T Polimorfizmlerinin İncelenmesi
SAĞLIK BİLİMLERİ DERGİSİ, cilt.15, ss.41-45, 2006 (Hakemli Üniversite Dergisi)
22q+ varyant ph1 kromozomlu bir kronik miyeloid lösemi olgusu.
Erciyes Üniversitesi Sağlık Bilimleri Dergisi, cilt.4, ss.42-45, 1995 (Hakemli Üniversite Dergisi)
Çeşitli antiseptik maddelerin değişik sürelerde cild florası üzerinde anti-mikrobiyal etkileri
ERCİYES TIP DERGİSİ, ss.246-249, 1995 (Hakemli Üniversite Dergisi)
22q+ Variant kromozomlu bir kronik miyeloid lösemi olgusu
Erciyes Üniversitesi Sağlık Bilimleri Dergisi, ss.42-45, 1995 (Hakemli Üniversite Dergisi)
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q
European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 May 2017, cilt.256
Retrospective results of 18 years prenatal diagnosis cases and its evaluation
European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 May 2017, cilt.256
The correlation of genotype-phenotype of FMF disease and its review of statistical data
European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 May 2017, cilt.256
Frequency of chromosome variants in families with recurrent pregnancy loss and statistical analysis of infertility
European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 May 2017, cilt.256
NF1 gene variant allele frequencies comparison of Turkish population with databases
European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 May 2017, cilt.256
Investigation of PAI-1 4G/5G Polymorphism In Turkish FMF Patients.
IX. Ulusal Tıbbi Genetik Kongresi., İstanbul, Türkiye, 1 - 04 December 2010
Kronik Böbrek Yetmezlikli Hastalarda PAI-1 Gen Polimorfizminin Araştırılması.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Türkiye, 1 - 04 May 2008
Ailesel Akdeniz Ateşi Olgularında Mutasyon Taranması.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Türkiye, 1 - 04 May 2008
Tromboz Eğilimi Olan Hastalarda Faktör V (G1691A), Protrombin (G20210A) ve MTHFR (C677T) Gen Mutasyonlarının Sıklığı.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Türkiye, 1 - 04 May 2008
No significant expression of Wt1 gene in multiple myeloma patients at diagnosis: Is Wt1 gene expression useful marker for minimal residual disease in multiple myeloma?
49th Annual Meeting of the American-Society-of-Hematology, Georgia, Amerika Birleşik Devletleri, 8 - 11 December 2007, cilt.110
Hangi İnfertil Olgularda AZF Gen Delesyonu ve Kromozom Anomalisi Varlığı Araştırılmalı?
7. Ulusal Androloji Kongresi, Ankara, Türkiye, 6 - 09 June 2007, ss.64
Gastrointestinal (GİS) Kanserlerinde MTHFR 677C-T, 1298A-G ve MTR 2756A-G Polimorfizmlerinin İncelenmesi
I. Tıbbi Onkoloji Kongresi, Antalya, Türkiye, 29 March - 02 April 2006, ss.98
Duchhene/Becker Musküler Distrofi Hastalarında Polimeraz Zincir Reaksiyonu İle Delesyon Analizi
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Türkiye, 1 - 04 May 2003