(Q45951160)

18 December 2017

title

Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene. (English)

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18 December 2017

author name string

Zhang L

1

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18 December 2017

Leeflang EP

2

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18 December 2017

Yu J

3

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18 December 2017

Arnheim N

4

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18 December 2017

language of work or name

English

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publication date

1 August 1994

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18 December 2017

published in

Nature Genetics

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18 December 2017

volume

7

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18 December 2017

issue

4

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18 December 2017

page(s)

531-535

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18 December 2017

Dynamic mutations: a new class of mutations causing human disease

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

A linkage map of microsatellite markers on the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

Triplet repeat mutations in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Triplet repeats strike again

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Mutation of human short tandem repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

How much do we know about spontaneous human mutation rates?

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Origin of the expansion mutation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-531

7 January 2021

Identifiers

DOI

10.1038/NG0894-531

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18 December 2017

Dimensions Publication ID

1000057273

0 references

1 reference

18 December 2017