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Noninvasive Test for Fragile X Syndrome, Using Hair Root Analysis

✍ Scribed by Rob Willemsen; Burcu Anar; Yolanda De Diego Otero; Bert B.A. de Vries; Yvonne Hilhorst-Hofstee; Arie Smits; Eddy van Looveren; Patrick J. Willems; Hans Galjaard; Ben A. Oostra


Book ID
117852895
Publisher
American Society of Human Genetics
Year
1999
Tongue
English
Weight
155 KB
Volume
65
Category
Article
ISSN
0002-9297

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## Abstract Molecular diagnosis of Fragile X Syndrome (FXS) is carried out by PCR or Southern blot analysis on DNA isolated from leukocytes. These DNA analyses are time consuming and expensive, making it impractical for mass screening programs. We have recently standardized and tested the diagnosti