FJ Probst, ER Roeder, VB Enciso, Z Ou, ML … - American journal of medical genetics. Part A, 2007 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
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Y Gu, DL Nelson - Cytogenet Genome Res, 2003 - content.karger.com The FMR2 gene is dysregulated by the fragile XE triplet repeat expansion in
patients with FRAXE mental retardation syndrome. A CCG triplet, located in the
5' untranslated region of the FRAXE gene undergoes expansion and ... Cited by 18 - Related articles - BL Direct - All 5 versions
B Coffee, M Ikeda, DB Budimirovic, LN … - American journal of medical genetics. Part A, 2008 - pubmedcentral.nih.gov The most common cause of fragile X syndrome is expansion of a CGG trinucleotide
repeat in the 5′UTR of FMR1. This expansion leads to transcriptional silencing
of the gene. However, other mutational mechanisms, such as deletions of ... Cited by 2 - Related articles - BL Direct - All 6 versions
[CITATION] Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including …
FJ Probst - American Journal of Medical Genetics Part A, 2007 - Wiley Subscription Services, Inc., A Wiley Company … Related articles
[CITATION] Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: A …
B Coffee - American Journal of Medical Genetics Part A, 2008 - Wiley Subscription Services, Inc., A Wiley Company … Related articles