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A new era of non‐invasive prenatal genetic diagnosis: exploiting fetal epigenetic differences
Author(s) -
Ladha S
Publication year - 2012
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2011.01835.x
Subject(s) - columbia university , citation , epigenetics , library science , genealogy , medicine , history , sociology , genetics , biology , media studies , computer science , gene
1. Papergeorgiou EA, Karagrigoriou A, Tsaliki E, Velissariou V, Carter NP, Patsalis PC. Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21. Nature Med 2011: 17: 510–513. 2. Society of Obstetricians and Gynaecologists of Canada. Canadian Guidelines for Prenatal Diagnosis. J Obstet Gynaecol Can 2001: 23: 616–624. 3. Rakyan VK, Down TA, Thorne NP et al. An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs). Genome Res 2008: 18: 1518–1529.