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Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
title
Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
main subject
Severe mental retardation
1 reference
based on heuristic
inferred from title
author name string
G C Webb
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
J L Halliday
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
D B Pitt
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
C G Judge
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
M Leversha
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
language of work or name
English
0 references
publication date
1 February 1982
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
page(s)
44-48
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
cites work
Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
X-linked mental retardation, macro-orchidism, and the Xq27 fragile site
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
X-linked mental retardation and an X-chromosome marker.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
Chromosome banding required for studies on X-linked mental retardation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
X-linked mental retardation associated with macro-orchidism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
Inherited congenital normofunctional testicular hyperplasia and mental deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
Familial X-linked mental retardation with an X chromosome abnormality
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
More on marker X chromosomes, mental retardation and macro-orchidism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
X-linked mental retardation with macro-orchidism and marker X chromosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
The importance of being a fragile site
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
The X-linked syndrome of macroorchidism and mental retardation: Further observations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048818
retrieved
21 June 2018
Identifiers
DOI
10.1136/JMG.19.1.44
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
PMCID
1048818
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
PubMed ID
7069746
1 reference
stated in
Europe PubMed Central
PMCID
1048818
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7069746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
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