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Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
title
Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
author name string
Sutherland GR
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Jacky PB
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Baker E
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Manuel A
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
language of work or name
English
0 references
publication date
1 May 1983
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
volume
35
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
page(s)
432-437
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
cites work
Heritable fragile sites on human chromosomes. VII. Children homozygous for the BrdU-requiring fra(10)(q25) are phenotypically normal
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=1685660
retrieved
28 September 2017
Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites
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=1685660
retrieved
28 September 2017
5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with 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=1685660
retrieved
28 September 2017
FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition
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=1685660
retrieved
28 September 2017
The fragile X chromosome.
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=1685660
retrieved
28 September 2017
Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics
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=1685660
retrieved
28 September 2017
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=1685660
retrieved
28 September 2017
Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6859039
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
[Genetic aspects of autosomal fragile sites. Apropos of 40 Cases]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6859039
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1685660
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
PubMed ID
6859039
1 reference
stated in
Europe PubMed Central
PMCID
1685660
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6859039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
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