De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints (Q30445573)

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English	De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints	scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints (English)

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

author name string

Warburton D

1

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

language of work or name

0 references

publication date

1 November 1991

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

49

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

5

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

995-1013

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Correlation between euploid structural chromosome rearrangements and mental subnormality in humans.

1 reference

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20 June 2018

An analysis of the break points of structural rearrangements in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Identification of translocation chromosomes by quinacrine fluorescence.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Forty four probands with an additional "marker" chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the European Collaborative Prenatal Diagnosis Centres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Inv dup (15): prenatal diagnosis and postnatal follow-up.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Incidence and significance of chromosomal translocations in prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Congenital chromosome breakage clusters within Giemsa-light bands and identifies sites of chromatin instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Outcome of de novo balanced translocations ascertained prenatally

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Comparative mapping of the constitutional and tumor-associated 11;22 translocations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Report of the committee on structural chromosome changes in neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Report of the committee on cytogenetic markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

How much difference does chromosome banding make? Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Marker chromosomes: cytogenetic characterization and 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=1683246

20 June 2018

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Correlation between phenotypic expression of de novo marker chromosomes and genomic organization using replicational banding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Mental retardation associated with "balanced" chromosome rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

Systematic analysis of 95 reciprocal translocations of autosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683246

20 June 2018

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 11q;22q translocation: a European collaborative analysis of 43 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antenatal diagnosis of a de novo paracentric inversion of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker chromosomes in a series of 10,000 prenatal diagnoses. Cytogenetic and follow-up studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Balanced chromosome rearrangements with abnormal phenotype]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of a reciprocal translocation t(5;11) (q11;p13) in a WAGR patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo Robertsonian D/D type translocations: the Leuven experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Possibly" de novo translocations: prenatal risk counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

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Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928105

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 September 2017

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