A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene

Author(s):  
Huilin Wang ◽  
Xiaofan Zhu ◽  
Baoheng Gui ◽  
Wan Chee Cheung ◽  
Mengmeng Shi ◽  
...  
2008 ◽  
Vol 132 (1) ◽  
pp. 95-98
Author(s):  
Bharat Thyagarajan ◽  
Matthew Bower ◽  
Michael Berger ◽  
Sidney Jones ◽  
Michelle Dolan ◽  
...  

Abstract Fragile X syndrome is the most common cause of inherited mental retardation among males. In most cases, the molecular basis of fragile X syndrome is the expansion and subsequent methylation of a CGG trinucleotide repeat in the 5′ untranslated region of the fragile X mental retardation 1 (FMR1) gene. Laboratory diagnosis usually relies on a combination of Southern blot and polymerase chain reaction analyses. In this case report we describe an unusual Southern blot result in a patient who presented with developmental delay and had a normal CGG repeat number by polymerase chain reaction analysis. Further investigation revealed a novel G3310C transversion in the FMR1 gene resulting in a new recognition site for the BssHII restriction enzyme. This novel restriction site could potentially mimic a partial deletion of the FMR1 gene on Southern blot analysis and thus represents a possible pitfall in the diagnosis of fragile X syndrome.


1994 ◽  
Vol 51 (4) ◽  
pp. 527-534 ◽  
Author(s):  
Gene Levinson ◽  
Anne Maddalena ◽  
Frances T. Palmer ◽  
Gary L. Harton ◽  
David P. Bick ◽  
...  

2012 ◽  
Vol 19 (3) ◽  
pp. 112-115 ◽  
Author(s):  
Reuven Sharony ◽  
Atalia Shtorch ◽  
Aliza Amiel ◽  
Esther Guetta ◽  
Leah Peleg ◽  
...  

2012 ◽  
Vol 16 (11) ◽  
pp. 1303-1308 ◽  
Author(s):  
Karen M. Carvalho Curtis-Cioffi ◽  
Debora Aparecida Rodrigueiro ◽  
Valter Curi Rodrigues ◽  
Regina M. Barretto Cicarelli ◽  
Raquel Mantuaneli Scarel-Caminaga

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