Literature DB >> 15750023

QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern Europe.

Marina Machatkova1, Martina Brouckova, Milada Matejckova, Alice Krebsova, Karl Sperling, Svetlana Vorsanova, Sergei Kutsev, Tatiana Zerova, Svetlana Arbuzova, Roman Krejci, Michael Petersen, Milan Macek.   

Abstract

Study of parental/meiotic origin of free trisomy 21 in nuclear families from Russia (70 cases), Ukraine (32 cases), and 22 from Germany revealed maternal nondisjunction in 77.3% (Germany), 93.8% (Ukraine), and 91.4% (Russia), paternal origin in 13.6%, 6.2%, and 8.6%, respectively. Maternal meiosis I errors were found in 84.4% (Ukraine), 77.1% (Russia), paternal origin in 3.1% (Ukraine), 2.9% (Russia). Maternal meiosis II errors occurred in 9.4% and 14.3% and paternal in 3.1% and 5.7% in Ukraine and Russia, respectively. No significant differences were found in maternal/paternal origin among Ukraine, Russia, Germany, and published data from other European regions.

Entities:  

Mesh:

Year:  2005        PMID: 15750023     DOI: 10.1369/jhc.4B6510.2005

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  2 in total

1.  Practical application of fluorescent quantitative PCR on Trisomy 21 in Chinese Han population.

Authors:  Xiaobo Sun; Ming Yan; Yuanzhen Zhang; Xin Zhou; Chunhong Wang; Fang Zheng; Chenling Xiong
Journal:  Mol Biol Rep       Date:  2006-09       Impact factor: 2.316

2.  Down syndrome: parental origin, recombination, and maternal age.

Authors:  Jadranka Vraneković; Ivana Babić Božović; Zorana Grubić; Jasenka Wagner; Dinko Pavlinić; Sophie Dahoun; Frédérique Bena; Vida Culić; Bojana Brajenović-Milić
Journal:  Genet Test Mol Biomarkers       Date:  2011-08-23
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.