(Q24680385)

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Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

intrauterine growth restriction

1 reference

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author name string

Robinson WP

1

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2 November 2019

Barrett IJ

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Bernard L

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Telenius A

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Bernasconi F

5

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Europe PubMed Central

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2 November 2019

Wilson RD

6

1 reference

Europe PubMed Central

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2 November 2019

Best RG

7

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Howard-Peebles PN

8

1 reference

Europe PubMed Central

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2 November 2019

Langlois S

9

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Europe PubMed Central

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2 November 2019

Kalousek DK

10

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2 November 2019

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1 April 1997

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Europe PubMed Central

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2 November 2019

American Journal of Human Genetics

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

60

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2 November 2019

4

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2 November 2019

917-927

1 reference

Europe PubMed Central

PMC publication ID

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2 November 2019

Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

7 April 2017

Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

7 April 2017

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

7 April 2017

Confined placental mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

7 April 2017

Chromosomal mosaicism confined to the placenta in human conceptions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

7 April 2017

Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Uniparental disomy for chromosome 16 in humans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Nondisjunction of chromosome 15: origin and recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

A somatic origin of homologous Robertsonian translocations and isochromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Maternal uniparental disomy 22 has no impact on the phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Confined placental mosaicism and stillbirth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Placental mosaicism and intrauterine survival of trisomies 13 and 18.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 September 2017

Mosaicism in chorionic villus sampling: an analysis of incidence and chromosomes involved in 2612 consecutive cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 November 2018

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 November 2018

Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712477

28 November 2018

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies of the aetiology of trisomy 8 in spontaneous abortions and the liveborn population

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of mosaicism in human placentae

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of nine pregnancies with confined placental mosaicism for trisomy 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confined chorionic mosaicism in prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaicism and accuracy of prenatal cytogenetic diagnoses after chorionic villus sampling and placental biopsies

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9106539

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9106539%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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