Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA Technology

2015 ◽  
Vol 126 (5) ◽  
pp. 1095-1099 ◽  
Author(s):  
Yuval Yaron ◽  
Jacques Jani ◽  
Maximilian Schmid ◽  
Dick Oepkes
Author(s):  
Francesca Romana Grati ◽  
Komal Bajaj ◽  
Giuseppe Simoni ◽  
Federico Maggi ◽  
Susan J. Gross ◽  
...  

2017 ◽  
Vol 44 (5) ◽  
pp. 330-346 ◽  
Author(s):  
Justin M. Burgener ◽  
Ariana Rostami ◽  
Daniel D. De Carvalho ◽  
Scott V. Bratman

2017 ◽  
Vol 37 (4) ◽  
pp. 420-422 ◽  
Author(s):  
Zhongxia Qi ◽  
Shreshtha Madaan ◽  
Shilpa Chetty ◽  
Jingwei Yu ◽  
Arun P. Wiita

2018 ◽  
Vol 55 (1) ◽  
pp. 55-70 ◽  
Author(s):  
Kristina V. Glebova ◽  
Natalya N. Veiko ◽  
Aleksey A. Nikonov ◽  
Lev N. Porokhovnik ◽  
Svetlana V. Kostuyk

2016 ◽  
Vol 40 (5) ◽  
Author(s):  
Dimo Dietrich

Abstract:Aberrant DNA methylation is a hallmark of malignancies and can be detected in circulating cell-free DNA (ccfDNA) in bodily fluids, i.e. blood plasma, serum and urine. The availability of technologies that allow for an accurate and sensitive quantification of ccfDNA DNA methylation enables the precise monitoring of dynamic pathologic processes and pharmacodynamics. Recently, the first ccfDNA methylation biomarker


2013 ◽  
Vol 35 (2) ◽  
pp. 177-181 ◽  
Author(s):  
Sylvie Langlois ◽  
Jo-Ann Brock ◽  
R. Douglas Wilson ◽  
François Audibert ◽  
Jo-Ann Brock ◽  
...  

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