نتایج جستجو برای: cytogenetic investigation

تعداد نتایج: 339100  

The most significant complication of pregnancy is recurrent miscarriage. Numerous factors have been described as associations with recurrent wastage such as: uterine abnormalities, immunological factors, endocrinologic imbalance and chromosomal defects. Cytogenetic evaluation of couples with recurrent pregnancy losses is performed on the basis of G-banding technique only after other possible et...

Journal: :iranian journal of cancer prevention 0
mohammed rafiq khan dept. of biotechnology, molecular diagnosis and drug discovery laboratory, school of life sciences, karpagam university, coimbatore, tamilnadu, india sellappa sudha dept. of biotechnology, molecular diagnosis and drug discovery laboratory, school of life sciences, karpagam university, coimbatore, tamilnadu, india

background: occupational and environmental exposures mostly represent mixtures of genotoxic agents, whereas the specificity of biomarker measurements varies widely. exploration of correlations among biomarkers contributes to the further progress of molecular cancer epidemiology and to the selection of the optimal biomarkers for the investigation of human exposure to carcinogens. the aim of this...

Down syndrome is one of the most common causes of mental retardation observed in approximately 1/700 live birth. The use of two or more STR markers related to chromosome 21 facilitates the diagnosis of Down syndrome within about six hours from the collection of the samples. This is the first study has been performed in Iranian population to assess the diagnostic value of using small tandem repe...

Akbar Safaei, Jahanbanoo Shahryari, Marzieh Hosseini Mohamad Reza Farzaneh Narjes Tabibi,

Background: Acute lymphoblastic leukemia (ALL) is the sixth most common malignancy in Iran. Cytogenetic analysis of leukemic blasts plays an important role in classification and prognosis in ALL patients. The purpose of this study was to define the frequency of chromosomal abnormalities of ALL patients in adults and children in Fars province, Iran.Methods: In this cross-sectional study, we eval...

Journal: :Genetics and molecular research : GMR 2006
Serap Tutgun Onrat Ferruh Aşçi Muhlis Ozkan

The karyotypes of water mites (Acari: Hydrachnellae: Hydrodromidae) are largely unknown. The present investigation is the first report of a study designed to characterize the chromosomes of water mites. The study was carried out with specimens of Hydrodroma despiciens collected from Eber Lake in Afyon, Turkey. Several different methods were tried to obtain chromosomes of this species. However, ...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2009
Beatriz Amstalden Barros Andréa Trevas Maciel-Guerra Maricilda Palandi De Mello Fernanda Borchers Coeli Annelise Barreto de Carvalho Nilma Viguetti-Campos Juliana de Godoy Assumpção Antonia Paula Marques-de-Faria Sofia Helena Valente de Lemos-Marini Gil Guerra-Junior

OBJECTIVE To evaluate the effect of the improvement of chromosome analysis on the cytogenetic findings of Turner syndrome (TS) patients. METHODS Retrospective study of the results of the karyotypes of 260 patients with TS, regarding banding techniques, number of cells analyzed and results of investigation of Y-chromosome sequences. According to karyotype, divided in 45,X; sex chromosome mosai...

2015
Na Rae Kim Sung-Hye Park

Central nervous system (CNS) neoplasms are the second most common childhood malignancy after leukemia and the most common solid organ neoplasm in children. Diagnostic dilemmas with small specimens from CNS neoplasms are often the result of multifactorial etiologies such as frozen or fixation artifact, biopsy size, or lack of knowledge about rare or unfamiliar entities. Since the late 1950s, ult...

2013
Diclehan ORAL Ayşegül TÜRKYILMAZ Selda SİMSEK

Nearly 60% of all first trimester spontaneous miscarriages are due to chromosomal abnormalities. The most frequent are numerical abnormalities (94%), followed by structural abnormalities(5%) and less frequently mosaicsm(1%). We report a 28 years-old couple in which an 4,8 translocation and 9 inversion has been identified during the investigation for recurrent miscarriages.They were phenotypical...

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