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English
Normal phenotype and partial trisomy for the G positive region of chromosome 21
scientific article published on June 1, 1979
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
title
Normal phenotype and partial trisomy for the G positive region of chromosome 21
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
main subject
trisomy
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
genetics
1 reference
stated in
Crossref
DOI
10.1136/JMG.16.3.227
reference URL
https://api.crossref.org/works/10.1136/JMG.16.3.227
retrieved
14 May 2022
author name string
A. Daniel
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
language of work or name
English
0 references
publication date
1 June 1979
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
full work available at URL
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/157396/pdf/?tool=EBI
file format
Portable Document Format
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/157396/?tool=EBI
file format
HTML
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
http://jmg.bmjjournals.com/cgi/content/abstract/16/3/227
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
https://europepmc.org/articles/PMC1012698
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
https://europepmc.org/articles/PMC1012698?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A157396
retrieved
14 May 2022
https://syndication.highwire.org/content/doi/10.1136/jmg.16.3.227
1 reference
stated in
Crossref
DOI
10.1136/JMG.16.3.227
reference URL
https://api.crossref.org/works/10.1136/JMG.16.3.227
retrieved
14 May 2022
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
volume
16
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
page(s)
227-229
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
cites work
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=1012698
retrieved
21 June 2018
Structure and inheritance of some heterozygous Robertsonian translocation in man
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=1012698
retrieved
21 June 2018
Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype
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=1012698
retrieved
21 June 2018
Down syndrome due to partial trisomy 21q
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=1012698
retrieved
21 June 2018
Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment 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=1012698
retrieved
21 June 2018
A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/157396
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial trisomy 21
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/157396
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.16.3.227
0 references
PMCID
1012698
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
PubMed ID
157396
1 reference
stated in
Europe PubMed Central
PubMed ID
157396
retrieved
24 July 2017
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