(Q35249493)

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Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326332%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326332%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

based on heuristic

inferred from title

fragile X syndrome

1 reference

based on heuristic

inferred from title

11

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6 November 2019

author name string

B B de Vries

1

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6 November 2019

A M van den Ouweland

2

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6 November 2019

S Mohkamsing

3

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6 November 2019

H J Duivenvoorden

4

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6 November 2019

E Mol

5

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6 November 2019

K Gelsema

6

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6 November 2019

M van Rijn

7

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6 November 2019

D J Halley

8

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6 November 2019

L A Sandkuijl

9

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6 November 2019

B A Oostra

10

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6 November 2019

M F Niermeijer

12

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6 November 2019

language of work or name

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publication date

1 September 1997

1 reference

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6 November 2019

American Journal of Human Genetics

1 reference

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6 November 2019

61

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6 November 2019

660-667

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6 November 2019

3

1 reference

Europe PubMed Central

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6 November 2019

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Population studies of the fragile X: a molecular approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

DNA testing for fragile X syndrome in schools for learning difficulties

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

The United Kingdom population with Down syndrome: present and future projections.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Population incidence and segregation ratios in the Martin-Bell syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Clinical screening score for the fragile X (Martin-Bell) syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

Population screening for fragile X

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

26 September 2018

Rapid antibody test for fragile X syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715962

26 September 2018

Prevalence of fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is it time for population-based prenatal screening for fragile-X?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population screening for fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population screening for fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population screening for fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Study supports screening for the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X screening: what is the real issue?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preventive screening for the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9326332

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326332%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326332%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9326332%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

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