Twelve families with fragile X(q27) (Q33673692)

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4 October 2019

title

Twelve families with fragile X(q27) (English)

1 reference

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4 October 2019

author name string

T Webb

series ordinal

1

1 reference

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4 October 2019

A Thake

series ordinal

2

1 reference

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4 October 2019

J Todd

series ordinal

3

1 reference

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4 October 2019

language of work or name

English

0 references

publication date

1 October 1986

1 reference

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Journal of Medical Genetics

4 October 2019

published in

1 reference

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4 October 2019

volume

23

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4 October 2019

issue

5

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4 October 2019

page(s)

400-406

1 reference

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Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation

4 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(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=1049775

Fragile X trait in a large kindred: transmission also through normal males

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

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=1049775

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

Marker X syndrome in an oriental family with probable transmission by a normal male.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

The fragile X chromosome in a large Indian kindred.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

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=1049775

Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049775

Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach

30 October 2018

1 reference

12 December 2020

Transmission of fragile (X) (q27) site from a male

1 reference

12 December 2020

Transmission of fragile (X)(q27) from normal male(s)

1 reference

12 December 2020

Randomized study for the treatment of adult advanced Hodgkin's disease: mechlorethamine, vincristine, procarbazine, and prednisone (MOPP) versus lomustine, vinblastine, and prednisone

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.23.5.400

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3783616%20AND%20SRC:MED&resulttype=core&format=json

4 October 2019

1 reference

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4 October 2019

PubMed publication ID

3783616

1 reference