Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study-Reference-Cited by-同舟云学术

Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

Published:2013-04 Issue:4 Volume:15 Page:290-298
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Inaba Yoshimi,Herlihy Amy S.,Schwartz Charles E.,Skinner Cindy,Bui Quang M.,Cobb Joanna,Shi Elva Z.,Francis David,Arvaj Alison,Amor David J.,Pope Kate,Wotton Tiffany,Cohen Jonathan,Hewitt Jacqueline K.,Hagerman Randi J.,Metcalfe Sylvia A.,Hopper John L.,Loesch Danuta Z.,Slater Howard R.,Godler David E.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2012134.pdf

Reference39 articles.

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3. DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome;International Journal of Molecular Sciences;2020-10-19

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5. Gene Copy Number Quantification of SHOX, VAMP7, and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates;Genetic Testing and Molecular Biomarkers;2020-06-01