Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? (Q33681527)

28 July 2017

title

Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? (English)

1 reference

28 July 2017

Zaragoza MV

1

1 reference

28 July 2017

Millie E

series ordinal

2

1 reference

28 July 2017

Redline RW

series ordinal

3

1 reference

28 July 2017

Hassold TJ

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1998

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

35

1 reference

28 July 2017

issue

11

1 reference

28 July 2017

page(s)

924-931

1 reference

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

28 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=1051486

Human aneuploidy: incidence, origin, and etiology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Recombination and nondisjunction in humans and flies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Diagnosis of complete molar pregnancy by microsatellites in archival material.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Scatter factor/hepatocyte growth factor is essential for liver development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Cytogenetic and molecular studies of Down syndrome individuals with leukemia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Growth factors, protooncogenes and human placental development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Molecular genetic analysis of complete hydatidiform moles

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Androgenetic origin of hydatidiform mole

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

Hydatidiform mole: two entities. A morphologic and cytogenetic study with some clinical consideration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051486

A cytogenetic study of 1000 spontaneous abortions

21 June 2018

1 reference

12 December 2020

Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform mole

1 reference

12 December 2020

Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions?

1 reference

12 December 2020

Genome imprinting phenomena on mouse chromosome 7

1 reference

12 December 2020

Parental origin of triploidy in human fetuses: evidence for genomic imprinting

1 reference

12 December 2020

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

1 reference

12 December 2020

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects

1 reference

12 December 2020

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.11.924

1 reference

28 July 2017

1 reference

28 July 2017

1 reference