Literature DB >> 12975794

Fetal diagnosis of monosomy X (Turner syndrome) with methylation-specific PCR.

Sérgio D J Pena, Rosane Sturzeneker.   

Abstract

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Year:  2003        PMID： 12975794     DOI： 10.1002/pd.675

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  2 in total

1.  A highly sensitive, high-throughput assay for the detection of Turner syndrome.

Authors:  Scott A Rivkees; Karl Hager; Seiyu Hosono; Anastasia Wise; Peining Li; Henry M Rinder; Jeffrey R Gruen
Journal:  J Clin Endocrinol Metab       Date:  2010-12-22       Impact factor: 5.958

2.  DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.

Authors:  Amit Sharma; Muhammad Ahmer Jamil; Nicole Nuesgen; Felix Schreiner; Lutz Priebe; Per Hoffmann; Stefan Herns; Markus M Nöthen; Holger Fröhlich; Johannes Oldenburg; Joachim Woelfle; Osman El-Maarri
Journal:  Clin Epigenetics       Date:  2015-07-28       Impact factor: 6.551
  2 in total

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