Literature DB >> 26622392

Genetic polymorphisms of short tandem repeat loci D13S305, D13S631 and D13S634 in the Han population of Tianjin, China.

Yunfang Shi1, Xiaozhou Li1, Duan Ju1, Yan Li1, Xiuling Zhang1, Ying Zhang1.   

Abstract

Short tandem repeat (STR) markers, also known as microsatellites, are extensively used in mapping studies, forensics and disease diagnosis due to their small dimension and low mutation and high polymorphism rates. In recent years quantitative fluorescence polymerase chain reaction (QF-PCR) has been successfully used to amplify STR markers in the prenatal diagnosis of common chromosomal abnormalities. This method provides a diagnosis of common aneuploidies 24-48 h after sampling with low error rates and cost; however, the size of different alleles, frequency, heterozygosity and distribution of STR markers vary among different populations. In the present study three STR markers, D13S305, D13S631 and D13S634, on chromosome 13 were analyzed in 350 unrelated individuals (200 males and 150 females) from the Han population of Tianjin, China using QF-PCR. Eleven, seven and 11 alleles of each marker were observed, respectively. The frequencies of the genotypes were in good agreement with Hardy-Weinberg equilibrium (P>0.05). The results showed that these three STR markers were highly polymorphic in the Han population of Tianjin, China. The study has provided basic data for use in the prenatal diagnosis of Patau syndrome.

Entities:  

Keywords:  Patau syndrome; quantitative fluorescence polymerase chain reaction; short tandem repeat

Year:  2015        PMID: 26622392      PMCID: PMC4509031          DOI: 10.3892/etm.2015.2560

Source DB:  PubMed          Journal:  Exp Ther Med        ISSN: 1792-0981            Impact factor:   2.447


  19 in total

1.  A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome.

Authors:  D W SMITH; K PATAU; E THERMAN; S L INHORN
Journal:  J Pediatr       Date:  1960-09       Impact factor: 4.406

2.  Development of quantitative-fluorescence polymerase chain reaction for the rapid prenatal diagnosis of common chromosomal aneuploidies in 1,000 samples in Singapore.

Authors:  S Baig; S S Y Ho; B L Ng; L Chiu; E S C Koay; G H Leow; L Gole; N Kothandaraman; J Chan; X Sun; Y H Chan; M Rauff; L L Su; A Biswas; M Choolani
Journal:  Singapore Med J       Date:  2010-04       Impact factor: 1.858

3.  QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region.

Authors:  Alison Hills; Celia Donaghue; Jonathan Waters; Katie Waters; Caroline Sullivan; Abhijit Kulkarni; Zoe Docherty; Kathy Mann; Caroline Mackie Ogilvie
Journal:  Prenat Diagn       Date:  2010-06       Impact factor: 3.050

Review 4.  Patau syndrome with a long survival (146 months): a clinical report and review of literature.

Authors:  Dimitrios Iliopoulos; Eleni Sekerli; Georgia Vassiliou; Vasiliki Sidiropoulou; Augerinos Topalidis; Despina Dimopoulou; Nikolaos Voyiatzis
Journal:  Am J Med Genet A       Date:  2006-01-01       Impact factor: 2.802

5.  Development of pentaplex PCR and genetic analysis of X chromosomal STRs in Punjabi population of Pakistan.

Authors:  Asif Nadeem; Masroor Ellahi Babar; Manzoor Hussain; Mohammad A Tahir
Journal:  Mol Biol Rep       Date:  2008-10-21       Impact factor: 2.316

6.  OmniPlex--a new QF-PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population.

Authors:  Martina Putzova; Lubomira Pecnova; Lucie Dvorakova; Inna Soldatova; Petr Goetz; David Stejskal
Journal:  Prenat Diagn       Date:  2008-12       Impact factor: 3.050

7.  Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.

Authors:  Huseyin Onay; Timur Ugurlu; Ayca Aykut; Sacide Pehlivan; Murat Inal; Sivekar Tinar; Cihangir Ozkinay; Ferda Ozkinay
Journal:  Gynecol Obstet Invest       Date:  2008-04-29       Impact factor: 2.031

Review 8.  Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies.

Authors:  Brigitte H W Faas; Vincenzo Cirigliano; The-Hung Bui
Journal:  Semin Fetal Neonatal Med       Date:  2011-04       Impact factor: 3.926

9.  Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria--estimation of applicability of 6 STR markers on chromosomes 21 and 18.

Authors:  Silvia Andonova; Radoslava Vazharova; Violeta Dimitrova; Valentina Mazneikova; Draga Toncheva; Ivo Kremensky
Journal:  Prenat Diagn       Date:  2004-03       Impact factor: 3.050

10.  Investigation of QF-PCR Application for Rapid Prenatal Diagnosis of Chromosomal Aneuploidies in Iranian Population.

Authors:  Habib Nasiri; Mohammad-Reza Noori-Dalooi; Jila Dastan; Saeed-Reza Ghaffari
Journal:  Iran J Pediatr       Date:  2011-03       Impact factor: 0.364

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  1 in total

1.  Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases.

Authors:  Zohreh Sharifi; Faezeh Rahiminejad; Atefeh Joudaki; Ameneh Sarhadi Bandehi; Hossein Farahzadi; Yeganeh Keshvar; Fatemeh Golnabi; Sanaz Naderi; Rasaneh Yazdani; Mehdi Shafaat; Shirin Ghadami; Maryam Abiri; Sirous Zeinali
Journal:  Sci Rep       Date:  2019-05-15       Impact factor: 4.379

  1 in total

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