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English
Additional evidence for fragile X activity in heterozygous carriers.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
title
Additional evidence for fragile X activity in heterozygous carriers
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
main subject
heterozygosity
1 reference
based on heuristic
inferred from title
author name string
Uchida IA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
Freeman VC
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
Jamro H
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
Partington MW
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
Soltan HC
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
language of work or name
English
0 references
publication date
1 September 1983
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
volume
35
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
issue
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
page(s)
861-868
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
cites work
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=1685813
retrieved
13 July 2018
Nonspecific X-linked mental retardation I: a review with information from 24 new families
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=1685813
retrieved
13 July 2018
Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of 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=1685813
retrieved
13 July 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=1685813
retrieved
13 July 2018
Activity of the fragile X in heterozygous carriers
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=1685813
retrieved
13 July 2018
Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium
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=1685813
retrieved
13 July 2018
Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives
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=1685813
retrieved
13 July 2018
X-linked mental retardation: a study of 7 families.
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=1685813
retrieved
26 September 2018
Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin.
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=1685813
retrieved
26 September 2018
Identifiers
PMC publication ID
1685813
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
PubMed publication ID
6614002
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685813
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6614002%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
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