نتایج جستجو برای: chromosomal

تعداد نتایج: 47372  

Journal: :international journal of reproductive biomedicine 0
razieh dehghani firoozabadi seyed mehdi klantar seyed mohammad seyed-hasani nasrin ghasemi maryam asgharnia mohammad hasan sheikhha

background: recurrent abortion is a difficult medical problem happening in about 1-2% of fertile women. most spontaneous miscarriages which happen in the first and second trimesters are caused by chromosomal abnormalities. objective: the present study tries to find the rate of chromosomal abnormalities in couples with recurrent pregnancy loss. materials and methods: in total 165 couples were re...

Journal: :international journal of fertility and sterility 0
maria maurer thomas ebner manuela puchner richard bernhard mayer omar shebl peter oppelt

background: selecting the best embryo for transfer, with the highest chance of achieving a vital pregnancy, is a major goal in current in vitro fertilization (ivf) technology. the high rate of embryonic developmental arrest during ivf treatment is one of the limitations in achieving this goal. chromosomal abnormalities are possibly linked with chromosomal arrest and selection against abnormal f...

Journal: :international journal of reproductive biomedicine 0
fadlalla elfateh ruixue wang zhihong zhang yuting jiang shuang chen ruizhi liu

background: wide range of disorders ranging from genetic disorders to coital difficulties can influence male fertility. in this regard, genetic factors are highlighted as the most frequent, contributed to 10-15%, of male infertility causes. objective: to investigate the influence of genetic abnormalities on semen quality and reproductive hormone levels of infertile men from northeast china. mat...

Journal: :international journal of reproductive biomedicine 0
sayee rajangam preetha tilak

background: division of human genetics (dhg) is a referral center for karyotyping and counseling to the couples as well as to the individuals referred with bad obstetric history and infertility. materials and methods: from 1972 to 2003, overall 1666 couples and 131 female partners with bad obstetric history (boh) such as; spontaneous abortions, live births with congenital malformations and stil...

Journal: :journal of family and reproductive health 0
habib nasiri department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i jila dastan iranian fetal medicine foundation, tehran, iran mohammad hasan seifi school of medicine, iran university of medical sciences, tehran, iran noori dalooi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i saeed reza ghaffari department of medical genetics, school of medicine, tehran university of medical sciences, tehran, i

objective: classic cell culture and karyotyping is routinely used for prenatal detection of different chromosomal abnormalities. molecular cytogenetic techniques have also recently been developed and used for this purpose. quantitative florescence pcr using short tandem repeat (str) markers has more potential for high throughput diagnosis. marker heterozygosity in short tandem repeats (str) is ...

Journal: :journal of midwifery and reproductive health 0
masoumeh kordi assistant professor, department of midwifery, evidence-based care research center, school of nursing and midwifery, mashhad university of medical sciences, mashhad, iran. sahar riazi msc student of midwifery, school of nursing and midwifery, mashhad university of medical sciences, mashhad, iran. marzieh lotfalizade associate professor, department of obstetrics and gynecologist, mashhad university of medical sciences, mashhad, iran. mohamad taghi shakeri professor, department of biostatistics, mashhad university of medical sciences, mashhad, iran.

introduction: the purpose of the screening of fetal anomalies in pregnancy is empowering women to make an informed choice and reduce uncertainty in decision making. on the other hand, screening may cause worry and anxiety in pregnant women. this study was conducted with aim to determine the relationship between informed choice in pregnant women about screening of fetal anomalies with worry and ...

Journal: :journal of dentistry, tehran university of medical sciences 0
f. agha-hosseini m. khazabb a. parvaneroo

statement of problem: many studies have indicated that genetic disturbances are common findings in patients with oral squamous cell carcinoma (oscc). identification of these changes can be helpful in diagnostic procedures of these tumors. purpose: the aim of this study was to appraise the chromosomal disorders in blood and tissue patients with oscc. methods and materials: in this descriptive st...

Journal: :medical journal of islamic republic of iran 0
h mozdarani from the dept. of radiology, school of medical sciences, tarbiat modarres university, po. box 14155- 4838, tehran, i.r. iran, fax. 8013030,8006544. mr tohidnia

application of nuclear magnetic resonance imaging (nmri) as a non-invasive and accurate imaging procedure has been widely used in recent years. meanwhile, the biological effects of magnetic fields of several tesla (t) and high energy radiofrequency (rf) is not fully known yet. because of controversy over this issue, the present research has been carried out in order to verify the effects of mag...

Journal: :iranian journal of biotechnology 2007
hassan motejadded josef altenbuchner

a new system is presented for the generation ofrecombinant bacillus subtilis strains without antibioticmarkers. this system is based on two plasmids constructed in escherichia coli. the first plasmid phm30contains an incomplete hisi gene, the last gene in thehistidine biosynthesis operon of b. subtilis and part ofthe genes yvca and yvcb of unkown function flankinghisi at the 3´-end. the spectin...

تابعی, سید محمد باقر, دیانت پور, مهدی, غفوری فرد, سوده, میریونسی, محمد,

Background: Mental retardation is defined as impaired mental capacity and ability to comply with environmental and social conditions. Chromosomal abnormalities are the most important causes of mental retardation. Carriers of balanced chromosomal translocation are phenotypically normal, although they may be at risk of infertility, recurrent miscarriage or giving birth to mentally retarded childr...

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