Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles. (Q50567156)

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scientific article published in July 2000

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English	Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.	scientific article published in July 2000

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scholarly article

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles. (English)

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

author name string

Larsen LA

1

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Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Armstrong JS

2

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Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Grønskov K

3

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Hjalgrim H

4

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Macpherson JN

5

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Brøndum-Nielsen K

6

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Hasholt L

7

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Nørgaard-Pedersen B

8

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Vuust J

9

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

publication date

1 July 2000

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Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

American Journal of Medical Genetics Part A

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Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

93

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http://europepmc.org/abstract/MED/10869110

2

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http://europepmc.org/abstract/MED/10869110

99-106

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

Examination of factors associated with instability of the FMR1 CGG repeat.

1 reference

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21 January 2018

Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat

1 reference

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Prenatal diagnosis and carrier screening for fragile X by PCR.

1 reference

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21 January 2018

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

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21 January 2018

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

1 reference

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21 January 2018

Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Population genetics of fragile X: a multiple allele model with variable risk of CGG repeat expansion.

1 reference

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21 January 2018

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

High-throughput analysis of fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation

1 reference

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21 January 2018

An n-allele model for progressive amplification in the FMR1 locus

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission

1 reference

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21 January 2018

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

1 reference

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21 January 2018

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

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21 January 2018

Frequency and stability of the fragile X premutation.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1002%2F1096-8628%2820000717%2993%3A2%3C99%3A%3AAID-AJMG4%3E3.0.CO%3B2-W

21 January 2018

Significance of linkage disequilibrium between the fragile X locus and its flanking markers

1 reference

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21 January 2018

Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spots

1 reference

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21 January 2018

Transmission of the FRAXA haplotype from three nonpenetrant brothers to their affected grandsons: an update with AGG interspersion analysis

1 reference

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21 January 2018

Evidence of founder chromosomes in fragile X syndrome

1 reference

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21 January 2018

Identifiers

10.1002/1096-8628(20000717)93:2<99::AID-AJMG4>3.0.CO;2-W

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

1 reference

Europe PubMed Central

15 March 2018

http://europepmc.org/abstract/MED/10869110

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