Confined placental mosaicism (Q24517911)

2 July 2017

1 reference

title

Confined placental mosaicism (English)

1 reference

2 July 2017

Kalousek DK

1

1 reference

2 July 2017

Vekemans M

series ordinal

2

1 reference

2 July 2017

language of work or name

English

0 references

publication date

1 July 1996

1 reference

Journal of Medical Genetics

2 July 2017

published in

1 reference

2 July 2017

volume

33

1 reference

2 July 2017

issue

7

1 reference

2 July 2017

page(s)

529-533

1 reference

Uniparental disomy as a mechanism for human genetic disease

2 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Origin of extraembryonic mesoderm in experimental animals: relevance to chorionic mosaicism in humans

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Chromosomal mosaicism confined to the placenta in human conceptions

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Uniparental disomy for chromosome 16 in humans.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

A chimaeric animal model for confined placental mosaicism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Implantation and the placenta: key pieces of the development puzzle

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Bloom syndrome and maternal uniparental disomy for chromosome 15.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

An audit of trisomy 16 in man.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Transgenes as molecular probes for genomic imprinting.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Placental mosaicism and intrauterine survival of trisomies 13 and 18.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

The differential roles of parental genomes in mammalian development.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Features of cell lineage in preimplantation mouse development

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Uniparental disomy: a rare consequence of the high rate of aneuploidy in human gametes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Chromosome mosaicism of the placenta--a cause of developmental failure of the fetus?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Mosaicism in chorionic villus sampling: an association with poor perinatal outcome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

Manufactured hexaparental mice show that adults are derived from three embyronic cells

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050657

A new genetic concept: uniparental disomy and its potential effect, isodisomy

29 November 2018

1 reference

12 December 2020

Confined chorionic mosaicism in prenatal diagnosis

1 reference

12 December 2020

Follow-up and pregnancy outcome after a diagnosis of mosaicism in CVS

1 reference

12 December 2020

Cytogenetic results from the U.S. Collaborative Study on CVS

1 reference

12 December 2020

Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples

1 reference

12 December 2020

Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation

1 reference

12 December 2020

NICHD conference. Genomic imprinting: consequences of uniparental disomy for human disease

1 reference

12 December 2020

The utilization of interphase cytogenetic analysis for the detection of mosaicism

1 reference

12 December 2020

Human maternal uniparental disomy for chromosome 16 and fetal development

1 reference

12 December 2020

An imprinted gene(s) for diabetes?

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.33.7.529

1 reference

OpenCitations bibliographic resource ID

2 July 2017

3900159

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3900159

1 reference