Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH. (Q33677339)

28 July 2017

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title

Small extra ring chromosome derived from chromosome 10p: clinical report and characterisation by FISH. (English)

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28 July 2017

Blennow E

1

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28 July 2017

Tillberg E

series ordinal

2

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28 July 2017

language of work or name

English

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publication date

1 May 1996

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28 July 2017

number of pages

4

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Journal of Medical Genetics

inferred from page(s)

published in

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28 July 2017

volume

33

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28 July 2017

issue

5

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28 July 2017

page(s)

399-402

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describes a project that uses

28 July 2017

fluorescence in situ hybridization

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Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

inferred from title

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Identification of marker chromosomes in thirteen patients using FISH probing

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Supernumerary chromosome marker (1) in a developmentally delayed child

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

A cytogenetic survey of 11,680 newborn infants

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

A small supernumerary marker chromosome X identified by in situ hybridization.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050610

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

30 October 2018

1 reference

12 December 2020

Extra marker chromosome in newborn children

1 reference

12 December 2020

Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses

1 reference

12 December 2020

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

1 reference

12 December 2020

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization

1 reference

12 December 2020

An imprinted gene(s) for diabetes?

1 reference

12 December 2020

A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samples

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12 December 2020

Identifiers

DOI

10.1136/JMG.33.5.399

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28 July 2017

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28 July 2017

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