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Yayın Arama

Toplam 27518 kayıt

Prenatal diagnosis of aneuploidies and microdelation/duplication in amniotic fluid and fetal aborted material by QF-PCR and MLPA analysis.
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2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Biomed Genet Genomics

A Prospective Case-Control Study Analyzes 12 Thrombophilic Gene Mutations in Turkish Couples with Recurrent Pregnancy Loss
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2010 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
American Journal of Reproductive Immunology

The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures.
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2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
European review for medical and pharmacological sciences

A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus
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2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Biomedical Genetics and Genomics

Fatma Sılan, Duygu Kankaya, Taner Karakaya, Baris Paksoy, Volkan Turunz and Ozturk Ozdemir.The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale.
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2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Biomedical Genetics and Genomics

The frequency of toll-like receptor 4 gene polymorphism in ankylosing spondylitis and its relationship between disease activity.
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2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
The European Research Journal

Çok Parametreli ve Çoklu Bilinmeyenli Kanser
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Türkiye Klinikleri Journal of Medical Genetics-Special Topics

Günümüzde Kanser Tanısında Kullanılan Geçerli ve Güvenilir Moleküler Tetkikler
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Turkiye Klinikleri Journal of Medical Genetics-Special Topics

Kanser Etyolojisinde Tetikleyici Moleküler Mekanizmalar
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Turkiye Klinikleri Journal of Medical Genetics-Special Topics

Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population.
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2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Clin Exp Dermatol.

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension
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2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
ANNALS OF SAUDI MEDICINE

Methylenetetrahydrofolate reductase gene germ-line C677T and A1298C SNPs are associated with colorectal cancer risk in the Turkish population
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2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Asian Pac J Cancer Prev

Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
BioDiscovery

A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2 , and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay
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2017 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
Journal of Biotechnology

A frameshift mutation in SLC34A2 gene in three patients with pulmonary alveolar microlithiasis in an inbread family
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2010 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
INTERNAL MEDICINE

Role of prothrombotic gene polymorphism in patients with thromboangiitis obliterans
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2009 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Türkiye Klinikleri Cardiovascular Sciences

Predictive significance of KRAS point mutation in patients with non small cell lung carcinoma relation to smoking and asbestos exposure in middle Anatolia population
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2010 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
HEALTHMED