(Q37219702)

English

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

scientific article published on 20 December 2002

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12497247%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

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

1 reference

Europe PubMed Central

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16 December 2019

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human pregnancy

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based on heuristic

inferred from title

Carolyn J. Brown

8

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16 December 2019

author name string

Beever CL

1

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16 December 2019

Stephenson MD

2

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16 December 2019

Peñaherrera MS

3

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16 December 2019

Jiang RH

4

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16 December 2019

Kalousek DK

5

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16 December 2019

Hayden M

6

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16 December 2019

Field L

7

1 reference

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16 December 2019

Robinson WP

9

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16 December 2019

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publication date

20 December 2002

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16 December 2019

American Journal of Human Genetics

1 reference

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16 December 2019

72

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16 December 2019

2

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16 December 2019

399-407

1 reference

Europe PubMed Central

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16 December 2019

Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

The origin of abnormalities in recurrent aneuploidy/polyploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Skewed X inactivation and recurrent spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

The causes and consequences of random and non-random X chromosome inactivation in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Recurrent pregnancy loss and diminished ovarian reserve

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Trisomic pregnancy and earlier age at menopause

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Ovarian differentiation and gonadal failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Proliferation and migration of primordial germ cells during compensatory growth in mouse embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Differential methylation of hypoxanthine phosphoribosyltransferase genes on active and inactive human X chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Absence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Methylation and sequence analysis around EagI sites: identification of 28 new CpG islands in XQ24-XQ28.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

6 September 2017

Chromosome anomalies as predictors of recurrence risk for spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

14 September 2017

Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

14 September 2017

Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

28 September 2017

Human aneuploidy: incidence, origin, and etiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

28 September 2017

A novel X chromosome-linked genetic cause of recurrent spontaneous abortion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

26 June 2018

Expand Long PCR for fragile X mutation detection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

26 June 2018

Maternal ageing and aneuploid embryos--evidence from the mouse that biological and not chronological age is the important influence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

26 June 2018

Ovarian dysgenesis in individuals with chromosomal abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

26 June 2018

Immune disorders in women with premature ovarian failure in initial period

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

3 September 2018

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

3 September 2018

Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379232

3 September 2018

X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12497247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reproductive outcome in patients with diminished ovarian reserve

1 reference

https://pubmed.ncbi.nlm.nih.gov/12497247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of factors associated with habitual abortion in 197 couples

1 reference

https://pubmed.ncbi.nlm.nih.gov/12497247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is the age of menopause determined in-utero?

1 reference

https://pubmed.ncbi.nlm.nih.gov/12497247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated day 3 serum follicle stimulating hormone and/or estradiol may predict fetal aneuploidy

1 reference

https://pubmed.ncbi.nlm.nih.gov/12497247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age- and tissue-specific variation of X chromosome inactivation ratios in normal women

1 reference

https://pubmed.ncbi.nlm.nih.gov/12497247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12497247%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12497247%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12497247%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

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