Trinucleotide repeat expansion and human disease
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,Analytical Chemistry
Reference92 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
2. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
3. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE
4. Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis
5. FRAGILE X SYNDROME: A UNIQUE MUTATION IN MAN
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3. Can VNTRs be used to study genetic variation within white spot syndrome virus isolates?;Journal of Fish Diseases;2010-05-06
4. Development of a pentaplex X-chromosomal short tandem repeat typing system and population genetic studies;Forensic Science International;2005-11
5. Highly informative nature of inter simple sequence repeat (ISSR) sequences amplified using tri- and tetra-nucleotide primers from DNA of cauliflower (Brassicaoleraceavar.botrytisL.);Genome;2002-10-01
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