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English
Familial Down syndrome: evidence supporting cytoplasmic inheritance
scientific article published on 01 December 2001
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
title
Familial Down syndrome: evidence supporting cytoplasmic inheritance
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
main subject
Down syndrome
1 reference
based on heuristic
inferred from title
supporting evidence
1 reference
based on heuristic
inferred from title
author
Svetlana Arbuzova
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
H Cuckle
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
R Mueller
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
I Sehmi
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 December 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
60
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
456-462
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
Down syndrome: genetic recombination and the origin of the extra chromosome 21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apolipoprotein E allele distribution in parents of Down's syndrome children.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nondisjunction in trisomy 21: origin and mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal age effect: The enigma of Down syndrome and other trisomic conditions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration a european collaborative study on prenatal diagnoses 1981
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk of recurrence of fetal chromosomal aberrations: analysis of trisomy 21, trisomy 18, trisomy 13, and 45,X in 1,076 Japanese mothers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrences of trisomy 18 and trisomy 13 after trisomy 21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE NONRANDOMNESS OF CHROMOSOMAL ABNORMALITIES. ASSOCIATION OF TRISOMY 18 AND DOWN'S SYNDROME
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Klinefelter's syndrome. Down's syndrome (Mongolism), and twinning in the same sibship
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Langdon Down anomaly (mongolism) with 21/21 translocation and Klinefelter's syndrome in the same sibship
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trisomy 21 Down syndrome. Parental mosaicism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple recurrence of trisomy 21 Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnancies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Double autosomal trisomy and mosaicism for chromosomes no. 8 and no. 21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Double trisomy in spontaneous abortions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down-Turner syndrome: case report and review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome abnormalities in human embryos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in diseases of energy metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High incidence of Down's syndrome in infants of diabetic mothers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased risk of Alzheimer's disease in mothers of adults with Down's syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-molecule analysis of DNA uncoiling by a type II topoisomerase.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A newly identified DNA ligase of Saccharomyces cerevisiae involved in RAD52-independent repair of DNA double-strand breaks
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.600609.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1034/J.1399-0004.2001.600609.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed publication ID
11846739
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11846739
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11846739%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
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