(Q33673680)

28 July 2017

title

The frequency of the fragile X chromosome among schoolchildren in Coventry (English)

1 reference

28 July 2017

Webb TP

1

1 reference

28 July 2017

Bundey S

series ordinal

2

1 reference

28 July 2017

Thake A

series ordinal

3

1 reference

28 July 2017

Todd J

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 October 1986

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

23

1 reference

28 July 2017

issue

5

1 reference

28 July 2017

page(s)

396-399

1 reference

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

Twelve families with fragile X(q27)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

Nonspecific X-linked mental retardation II: the frequency in British Columbia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049774

Heritable fragile sites on human chromosomes. XII. Population cytogenetics

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3783615

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1049774

1 reference

28 July 2017

1 reference