Methylation analysis in newborn screening for fragile X syndrome
JAMA Neurol
.
2014 Jun;71(6):800.
doi: 10.1001/jamaneurol.2014.142.
Authors
David E Godler
1
,
David J Amor
1
,
Howard R Slater
1
Affiliation
1
The Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne/Parkville, Victoria, Australia.
PMID:
24911126
DOI:
10.1001/jamaneurol.2014.142
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
Comment
MeSH terms
Fragile X Syndrome / diagnosis*
Genetic Testing / standards*
Humans
Neonatal Screening / standards*