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Cytogenetic and molecular studies of trisomy 13.
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
title
Cytogenetic and molecular studies of trisomy 13
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
author name string
T Hassold
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
P A Jacobs
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
M Leppert
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
M Sheldon
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
language of work or name
English
0 references
publication date
1 December 1987
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
volume
24
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
issue
12
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
page(s)
725-732
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
cites work
Maternal-age effect in aneuploidy: does altered embryonic selection play a role?
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=1050401
retrieved
21 June 2018
Chiasma frequency and maternal age in mammals.
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=1050401
retrieved
21 June 2018
Further studies on bivalent chiasma frequency in human males with normal karyotypes.
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=1050401
retrieved
21 June 2018
The relationship between maternal age and chromosome size in autosomal trisomy
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=1050401
retrieved
21 June 2018
A primary genetic map of chromosome 13q.
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=1050401
retrieved
21 June 2018
Trisomy 13 ascertained in a survey of spontaneous abortions
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=1050401
retrieved
21 June 2018
Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms
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=1050401
retrieved
21 June 2018
Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences 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=1050401
retrieved
21 June 2018
Detection of specific sequences among DNA fragments separated by gel electrophoresis
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=1050401
retrieved
21 June 2018
Origin of human trisomics and polyploids
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=1050401
retrieved
21 June 2018
Estimating distances from the centromere by means of benign ovarian teratomas in man
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2892938
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Parental origin of de novo chromosome rearrangements
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2892938
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2892938
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Parental origin of autosomal trisomies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2892938
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Origin of extra chromosome in Patau syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2892938
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Reduced recombination rate on chromosomes 21 that have undergone nondisjunction
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2892938
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.24.12.725
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
PMC publication ID
1050401
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
PubMed publication ID
2892938
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050401
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2892938%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
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