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A chromosome 21 critical region does not cause specific Down syndrome phenotypes.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
title
A chromosome 21 critical region does not cause specific Down syndrome phenotypes
(English)
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
main subject
Down syndrome
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author
Lisa E Olson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
author name string
J T Richtsmeier
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
J Leszl
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
R H Reeves
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
language of work or name
English
0 references
publication date
1 October 2004
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
published in
Science
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
volume
306
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
issue
5696
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
page(s)
687-690
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
cites work
Too much of a good thing: mechanisms of gene action in Down 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=4019810
retrieved
21 June 2018
The DNA sequence of human chromosome 21
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=4019810
retrieved
21 June 2018
Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities
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=4019810
retrieved
21 June 2018
Down syndrome phenotypes: the consequences of chromosomal imbalance
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=4019810
retrieved
21 June 2018
Molecular mapping of twenty-four features of Down syndrome on chromosome 21.
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=4019810
retrieved
21 June 2018
Chromosome engineering in mice
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=4019810
retrieved
21 June 2018
Down syndrome—a disruption of homeostasis
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=4019810
retrieved
21 June 2018
Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.
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=4019810
retrieved
21 June 2018
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.
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=4019810
retrieved
21 June 2018
Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions
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=4019810
retrieved
30 October 2018
Protection from doxorubicin-induced cardiac toxicity in mice with a null allele of carbonyl reductase 1
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=4019810
retrieved
30 October 2018
A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome.
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=4019810
retrieved
30 October 2018
Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.
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=4019810
retrieved
30 October 2018
Identifiers
DOI
10.1126/SCIENCE.1098992
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
PMCID
4019810
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
PubMed ID
15499018
1 reference
stated in
Europe PubMed Central
PMCID
4019810
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15499018%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 January 2020
ResearchGate publication ID
8218173
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