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To err (meiotically) is human: the genesis of human aneuploidy
scientific article (publication date: April 2001)
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title
To err (meiotically) is human: the genesis of human aneuploidy
(English)
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PubMed
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11283700
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30 April 2017
author name string
Hassold T
series ordinal
1
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PubMed
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30 April 2017
Hunt P
series ordinal
2
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PubMed
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30 April 2017
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English
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30 April 2017
publication date
April 2001
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30 April 2017
published in
Nature Reviews Genetics
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PubMed
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30 April 2017
volume
2
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30 April 2017
page(s)
280-91
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PubMed
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11283700
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30 April 2017
issue
4
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PubMed
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11283700
retrieved
30 April 2017
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Meiotic recombination and segregation of human-derived artificial chromosomes in Saccharomyces cerevisiae
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The meiotic competence of in-vitro matured human oocytes is influenced by donor age: evidence that folliculogenesis is compromised in the reproductively aged ovary.
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Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21
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Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
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The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
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Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns
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Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology?
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Exchanges are not equally able to enhance meiotic chromosome segregation in yeast
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Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories.
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A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin
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Crossref
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Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination
1 reference
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Crossref
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Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors
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Predivision in human oocytes at meiosis I: a mechanism for trisomy formation in man.
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Crossref
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First-meiotic-division nondisjunction in human oocytes
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Crossref
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Chromosome anomalies in human oocytes in relation to age.
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Crossref
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7 January 2021
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Maternal age and trisomy--a unifying mechanism of formation.
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Crossref
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Maternal age in trisomy
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Crossref
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7 January 2021
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Trisomic pregnancy and earlier age at menopause
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Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome
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Oocyte selection: a new model for the maternal-age dependence of Down syndrome
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Requirement of the spindle checkpoint for proper chromosome segregation in budding yeast meiosis
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The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility
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Chromosome abnormalities in oral contraceptive breakthrough pregnancies
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7 January 2021
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The teratogenic effects of alcohol following exposure during pregnancy, and its influence on the chromosome constitution of the pre-ovulatory egg.
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Seasonality of pre-ovulatory non-disjunction and the aetiology of Down syndrome. A European collaborative study
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Crossref
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Increased parity and risk of trisomy 21: review of 37,110 live births
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Crossref
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7 January 2021
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High incidence of Down's syndrome in infants of diabetic mothers
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Apolipoprotein E allele distribution in parents of Down's syndrome children.
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Down syndrome and ionizing radiation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Trisomy in man
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is there evidence of clustering in Down syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Down's syndrome in infants of diabetic mothers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Seasonal variation in the prevalence of Down syndrome at birth: a review
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Apolipoprotein E epsilon 4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of nucleolar organizing regions in parents of trisomic spontaneous abortions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal smoking and Down syndrome: the confounding effect of maternal age
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk factors for trisomy 21: maternal cigarette smoking and oral contraceptive use in a population-based case-control study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35066065
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/35066065
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11283700
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
140182
Dimensions Publication ID
1014669459
0 references
OpenCitations bibliographic resource ID
140182
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
140182
PubMed ID
11283700
2 references
stated in
PubMed
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=11283700
retrieved
30 April 2017
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
140182
ResearchGate publication ID
12049418
0 references
Springer Nature article ID
10.1038/35066065
0 references
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