(Q43075544)

13 November 2017

High resolution comparative genomic hybridisation in clinical cytogenetics (English)

1 reference

13 November 2017

1 reference

Kirchhoff M

1

1 reference

13 November 2017

Rose H

series ordinal

2

1 reference

13 November 2017

Lundsteen C

series ordinal

3

1 reference

13 November 2017

language of work or name

English

0 references

publication date

1 November 2001

1 reference

Journal of Medical Genetics

13 November 2017

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13 November 2017

38

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13 November 2017

11

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13 November 2017

740-744

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Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissue

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Subtle chromosomal rearrangements in children with unexplained mental retardation

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridization

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Absence of predictable phenotypic expression in proximal 15q duplications

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Cryptic familial t(11;18)(q25;q23) incidentally detected by interphase FISH.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Comparative genomic hybridization for cytogenetic evaluation of stillbirth

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Automatic correction of the interfering effect of unsuppressed interspersed repetitive sequences in comparative genomic hybridization analysis.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734756

Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study

3 November 2018

1 reference

12 December 2020

High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes

1 reference

12 December 2020

Clinical applications of comparative genomic hybridization

1 reference

12 December 2020

Two unusual G-band variants of the short arm of chromosome 9

1 reference

12 December 2020

"Possibly" de novo translocations: prenatal risk counseling

1 reference

12 December 2020

Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals

1 reference

12 December 2020

Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization

1 reference

12 December 2020

Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q

1 reference

12 December 2020

Deletions below 10 megabasepairs are detected in comparative genomic hybridization by standard reference intervals

1 reference

12 December 2020

Comparative genomic hybridization: a new approach to screening for intrauterine complete or mosaic aneuploidy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.38.11.740

1 reference

13 November 2017

1 reference

13 November 2017

PubMed publication ID

11694545

1 reference