(Q40743758)

23 September 2017

Standardization of PCR amplification for fragile X trinucleotide repeat measurements (English)

1 reference

23 September 2017

O'Connell CD

1

1 reference

23 September 2017

Atha DH

2

1 reference

23 September 2017

Jakupciak JP

3

1 reference

23 September 2017

Amos JA

4

1 reference

23 September 2017

Richie K

5

1 reference

23 September 2017

1 January 2002

1 reference

23 September 2017

1 reference

23 September 2017

61

1 reference

23 September 2017

1

1 reference

23 September 2017

13-20

1 reference

Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures

23 September 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Tissue-specific methylation differences in a fragile X premutation carrier.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Advances in molecular analysis of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Fragile sites and minisatellite repeat instability

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Rethinking genotype and phenotype correlations in polyglutamine expansion disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Flexible DNA: genetically unstable CTG.CAG and CGG.CCG from human hereditary neuromuscular disease genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

CTG triplet repeats from the myotonic dystrophy gene are expanded in Escherichia coli distal to the replication origin as a single large event.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610103.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2002.610103.X

1 reference

23 September 2017

1 reference