Trisomy recurrence: a reconsideration based on North American data (Q30943096)

16 October 2017

Trisomy recurrence: a reconsideration based on North American data (English)

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16 October 2017

1

Dorothy Warburton

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16 October 2017

2

Louis Dallaire

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16 October 2017

Maya Thangavelu

3

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16 October 2017

Lori Ross

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4

1 reference

16 October 2017

Bruce Levin

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5

1 reference

16 October 2017

Jennie Kline

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6

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16 October 2017

language of work or name

English

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publication date

8 July 2004

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American Journal of Human Genetics

16 October 2017

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16 October 2017

75

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16 October 2017

3

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16 October 2017

376-385

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Bisphenol a exposure causes meiotic aneuploidy in the female mouse

16 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Meiotic cohesion requires accumulation of ORD on chromosomes before condensation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

To err (meiotically) is human: the genesis of human aneuploidy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Trisomic pregnancy and earlier age at menopause

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

DNA polymorphism analysis in families with recurrence of free trisomy 21

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Rates of trisomy 18 in livebirths, stillbirths, and at amniocentesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Fetal loss in Down syndrome pregnancies

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182017

Maternal age-specific risks for trisomies at 9-14 weeks' gestation

25 November 2018

1 reference

12 December 2020

Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21

1 reference

12 December 2020

What is the true fetal loss rate in pregnancies affected by trisomy 21 and how does this influence whether first trimester detection rates are superior to those in the second trimester?

1 reference

12 December 2020

Familial Down syndrome: evidence supporting cytoplasmic inheritance

1 reference

12 December 2020

Covariation of synaptonemal complex length and mammalian meiotic exchange rates

1 reference

12 December 2020

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

12 December 2020

Trisomy 21 Down syndrome. Parental mosaicism

1 reference

12 December 2020

Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnancies

1 reference

12 December 2020

Maternal age- and gestation-specific risk for trisomy 21

1 reference

12 December 2020

Trisomy 21 mosaicism in gonads with unexpectedly high recurrence risks

1 reference

12 December 2020

Identifiers

DOI

10.1086/423331

1 reference

16 October 2017

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16 October 2017

PubMed publication ID

15248154

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