نتایج جستجو برای: azeri turkish

تعداد نتایج: 20399  

Mahmood Shekari Khaniani Nahid Karimian Fathi Sima Mansoori Derakhshan Vahid Montazeri,

Objective(s): Breast cancer is the most common cancer in women. Every year, one million new cases are reported worldwide, representing 18% of the total number of cancer in women. Hereditary BRCA1 and BRCA2 mutations account for about 60% of inherited breast cancer and are the only known causes of hereditary breast cancer syndrome. The aim of this study was to determine the frequency of BRCA2 (e...

Journal: :iranian journal of basic medical sciences 0
nahid karimian fathi medical genetic department medical faculty, tabriz university of medical sciences, tabriz, iran mahmood shekari khaniani medical genetic department medical faculty, tabriz university of medical sciences, tabriz, iran vahid montazeri general surgery department medical faculty, tabriz university of medical sciences, tabriz, iran sima mansoori derakhshan medical genetic department medical faculty, tabriz university of medical sciences, tabriz, iran

objective(s): breast cancer is the most common cancer in women. every year, one million new cases are reported worldwide, representing 18% of the total number of cancer in women. hereditary brca1 and brca2 mutations account for about 60% of inherited breast cancer and are the only known causes of hereditary breast cancer syndrome. the aim of this study was to determine the frequency of brca2 (e...

2012
Amir Shojaei

This research tries to investigate and identify firstly some existing obstacles in the process of translating inter-lingual idiomatic pairs, and then to suggest some weighty theoretical strategies to overcome such difficulties. Following Mona Baker's (1992) classification of difficulties and strategies and the related subcategories mentioned, the present study makes an effort to analyze such cl...

2015
Jalal Gharesouran Azizeh Farshbaf Khalili Noushin Sorkhkoh Azari Leila Vahedi

Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene encoding methyl-CpG binding protein 2 (MECP2). Clinical manifestations include neurodevelopmental disorder characterized by early-onset intractable seizures, severe developmental delay, intellectual disability, and abnormal electroencephalograms. Afflicted females show normal development until the ...

2015
Morteza Bagheri Isa Abdi Rad Nima Hosseini Jazani Rasoul Zarrin Ahad Ghazavi

BACKGROUND The variable numbers of tandem-repeat (VNTR) alleles at the phenylalanine hydroxylase (PAH) gene have been used in carrier detection and prenatal diagnosis in phenylketonuria families. This study was carried out to analyze VNTR alleles at the PAH gene in Iranian Azeri Turkish population. METHODS In this study, 200 alleles from general population were studied by PCR. RESULTS The f...

Journal: :Journal of medical genetics 1994
A M Kuliev I M Rasulov T Dadasheva E I Schwarz C Rosatelli L Saba A Meloni E Gemidjioglu M Petrou B Modell

beta thalassaemia is present throughout the southern regions of the former USSR. We have defined the clinical picture of the disorder, the spectrum of beta thalassaemia mutations, and the role of customary consanguineous marriage in Azerbaijan, where thalassaemia presents a public health problem of the same order as that in Greece. Contrary to earlier suggestions, we found that the common form ...

2014
Mortaza Bonyadi Reza Abdolmohammadi Zohreh Jahanafrooz Mohammad-Hosein Somy Manoochehr Khoshbaten

CONTEXT Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory diseases of the bowel (IBD) whose causes are not fully known. Emerging data indicate that alterations in cytokine synthesis may play a role in IBD pathogenesis. AIMS We aimed to determine the association between tumor necrosis factor-alfa (TNFα) promoter polymorphisms (at positions - 308 and - 1031) and suscepti...

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