Polymerase chain reaction analysis as a rapid screening test for diagnosis of fragile X syndrome

Fragile X syndrome is a result of an unstable expansion of (CGG)n trinucleotide sequences in the FMR-1 (Fragile X Mental Retardation 1) gene site at Xq27. In a normal person, n ranges from 6 to 40 repeats with an average of 30 repeats, whereas in a mutated FMR1 gene the sequence is repeated several...

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Bibliographic Details
Main Authors: Phan CL (Author), Zubaidah Z (Author), Gregory A.R.A (Author), Kamariah MN (Author), Ten SK (Author), Maimonah R (Author), Thilagavathi S (Author)
Format: Article
Language:English
Published: Penerbit UKM, 2006.
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