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English
De novo tandem duplication 17p11 leads to cen.
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
title
De novo tandem duplication 17p11 leads to cen.
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
author name string
Docherty Z
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
Hultén MA
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
Honeyman MM
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 April 1983
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
volume
20
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
page(s)
138-142
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
issue
2
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stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
cites work
An extra small metacentric chromosome identified as a deleted chromosome No. 17
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=1049020
retrieved
21 June 2018
The production of micronuclei from chromosome aberrations in irradiated cultures of human lymphocytes
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=1049020
retrieved
21 June 2018
A case of partial trisomy 17 resulting from X-autosomal translocation
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=1049020
retrieved
21 June 2018
Partial duplication of 17p. A new chromosomal 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=1049020
retrieved
21 June 2018
Trisomy of the short arm of chromosome 17
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842549
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pure trisomy 17p in 60% cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6842549
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.20.2.138
0 references
PMCID
1049020
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
PubMed ID
6842549
1 reference
stated in
Europe PubMed Central
PubMed ID
6842549
retrieved
28 July 2017
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