(Q37310009)

19 August 2017

The fragile X prevalence paradox (English)

1 reference

19 August 2017

Paul J Hagerman

1

1 reference

PMC publication ID

2728763

19 August 2017

language of work or name

English

0 references

publication date

15 April 2008

1 reference

Journal of Medical Genetics

19 August 2017

1 reference

19 August 2017

45

1 reference

19 August 2017

8

1 reference

19 August 2017

498-499

1 reference

Fragile X-associated tremor/ataxia syndrome: an aging face of the fragile X gene.

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Size bias of fragile X premutation alleles in late-onset movement disorders.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Lessons from fragile X regarding neurobiology, autism, and neurodegeneration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Screening for fragile X syndrome: a literature review and modelling study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Mental status of females with an FMR1 gene full mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Prevalence of the fragile X syndrome in African-Americans

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728763

Screening for fragile X syndrome in women of reproductive age

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18413371

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2008.059055

1 reference

19 August 2017

1 reference

PMC publication ID

2728763

19 August 2017

PubMed publication ID

18413371

1 reference

PMC publication ID

2728763