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Molecular studies of trisomy 18
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Molecular studies of trisomy 18
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
author name string
Fisher JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
Harvey JF
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
Lindenbaum RH
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
Boyd PA
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
Jacobs PA
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
language of work or name
English
0 references
publication date
1 June 1993
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
volume
52
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
page(s)
1139-1144
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
cites work
EXCHANGE AND NONDISJUNCTION OF THE X CHROMOSOMES IN FEMALE DROSOPHILA MELANOGASTER
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=1682277
retrieved
13 July 2018
A new trisomic syndrome
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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=1682277
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13 July 2018
Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Trisomy 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=1682277
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13 July 2018
A genetic linkage map of the human genome.
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PubMed Central
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13 July 2018
A simple salting out procedure for extracting DNA from human nucleated cells
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
The heteromorphic marker on chromosome 18 using restriction endonuclease AluI.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
An anonymous single copy chromosome 18 probe associated with a frequent RFLP (D18S5).
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Cytogenetic and molecular studies of trisomy 13.
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13 July 2018
A frequent Pvu II RFLP of the human gastrin releasing peptide gene
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Parental origin of the extra chromosome in trisomy 18.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8).
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=1682277
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13 July 2018
Systematic cloning of human minisatellites from ordered array charomid libraries.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682277
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13 July 2018
A centromere map of the X chromosome from trisomies of maternal origin
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=1682277
retrieved
13 July 2018
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
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=1682277
retrieved
13 July 2018
Trisomy 21: association between reduced recombination and nondisjunction
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=1682277
retrieved
13 July 2018
The meiotic stage of nondisjunction in trisomy 21: determination by using DNA 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=1682277
retrieved
13 July 2018
Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP)
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=1682277
retrieved
13 July 2018
Incidence of chromosome aberrations among 11 148 newborn children
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=1682277
retrieved
13 July 2018
Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A microsatellite genetic linkage map of human chromosome 18
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
SAM 1.1 and JOSH 4.4: two RFLPs within the human DCC gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Maternal age in trisomy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Sex ratio in spontaneous abortions
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8503446
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1682277
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
PubMed publication ID
8503446
1 reference
stated in
Europe PubMed Central
PMC publication ID
1682277
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8503446%20AND%20SRC:MED&resulttype=core&format=json
retrieved
13 October 2019
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