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English
Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting.
scientific article published in October 1998
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
title
Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author
Anne Ferguson-Smith
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author name string
P Georgiades
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
C Chierakul
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
language of work or name
English
0 references
publication date
1 October 1998
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
35
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
issue
10
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
821-824
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
cites work
Paternal uniparental disomy for chromosome 14: a case report and review
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=1051456
retrieved
21 June 2018
A somatic origin of homologous Robertsonian translocations and isochromosomes.
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=1051456
retrieved
21 June 2018
Distal duplication 14q: report of three cases and further delineation of the syndrome.
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=1051456
retrieved
21 June 2018
Terminal deletion of the long arm of chromosome 10: case report and review of the literature
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=1051456
retrieved
21 June 2018
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty.
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=1051456
retrieved
30 October 2018
Distal trisomy 14q syndrome; a case report.
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=1051456
retrieved
30 October 2018
Duplication of the distal segment of 14q
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=1051456
retrieved
30 October 2018
Partial deletion of 14q and partial duplication of 14q in sibs: testicular mosaicism for t(14q;14q) as a common mechanism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9783704
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.35.10.821
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PMC publication ID
1051456
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
9783704
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051456
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9783704%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
ResearchGate publication ID
13502061
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