(Q45302059)

11 December 2017

Polymorphisms in the CAG repeat--a source of error in Huntington disease DNA testing (English)

1 reference

11 December 2017

0 references

Yu S

1

1 reference

11 December 2017

Fimmel A

series ordinal

2

1 reference

11 December 2017

Fung D

series ordinal

3

1 reference

11 December 2017

Trent RJ

series ordinal

4

1 reference

11 December 2017

1 December 2000

1 reference

11 December 2017

1 reference

11 December 2017

58

1 reference

11 December 2017

6

1 reference

11 December 2017

469-472

1 reference

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

11 December 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

Two novel single-base-pair substitutions adjacent to the CAG repeat in the huntington disease gene (IT15): implications for diagnostic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

Laboratory Guidelines for Huntington Disease Genetic Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580607.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2000.580607.X

1 reference

11 December 2017

1 reference