(Q33596892)

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Prevalence of fragile X syndrome

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1865479

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28 July 2017

title

Prevalence of fragile X syndrome (English)

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Europe PubMed Central

PubMed publication ID

28 July 2017

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Webb T

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1865479

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28 July 2017

Bundey S

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1865479

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28 July 2017

language of work or name

English

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publication date

1 May 1991

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28 July 2017

published in

Journal of Medical Genetics

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28 July 2017

volume

28

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1865479

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28 July 2017

issue

5

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1865479

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28 July 2017

page(s)

358

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1865479

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28 July 2017

cites work

A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016861

retrieved

21 June 2018

The frequency of the fragile X chromosome among schoolchildren in Coventry

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016861

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21 June 2018

Children with the fragile X chromosome at schools for the mildly mentally retarded.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016861

retrieved

21 June 2018

The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016861

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30 October 2018

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DOI

10.1136/JMG.28.5.358

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Europe PubMed Central

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1865479

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28 July 2017

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release_fwr3yyngjjb4hnosp3qqgxtpca

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24 November 2022

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PMC publication ID

1016861

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Europe PubMed Central

PubMed publication ID

1865479

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28 July 2017

PubMed publication ID

1865479

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Europe PubMed Central

PubMed publication ID

1865479

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28 July 2017

ResearchGate publication ID

21289464

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(Q33596892)

Prevalence of fragile X syndrome

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