(Q37600444)

21 August 2017

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

1 reference

21 August 2017

1 reference

1 reference

1

Morton NE

1 reference

21 August 2017

Macpherson JN

2

1 reference

PMCID

525664

21 August 2017

language of work or name

English

0 references

publication date

1 May 1992

1 reference

Proceedings of the National Academy of Sciences of the United States of America

21 August 2017

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21 August 2017

89

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21 August 2017

4215-4217

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21 August 2017

9

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Distribution of Induced Breaks along the X-Chromosome of Drosophila Melanogaster

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Autosomal suppressor gene for fragile-X: an hypothesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Fragile-X mutation proposed to block complete reactivation in females of an inactive X chromosome

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

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

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

Absence of expression of the FMR-1 gene in fragile X syndrome

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

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

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

The marker (X) syndrome: a cytogenetic and genetic analysis.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=525664

1 September 2018

Identifiers

DOI

10.1073/PNAS.89.9.4215

1 reference

21 August 2017

0 references

1 reference

21 August 2017

1 reference

PMCID

525664