(Q34510648)

2 August 2017

New cytogenetically visible copy number variant in region 8q21.2. (English)

1 reference

2 August 2017

Marina Manvelyan

1

1 reference

2 August 2017

Friedrich W Cremer

2

1 reference

2 August 2017

Jeannette Lancé

3

1 reference

2 August 2017

Rüdiger Kläs

4

1 reference

2 August 2017

Christina Kelbova

5

1 reference

2 August 2017

Christian Ramel

6

1 reference

2 August 2017

Herbert Reichenbach

7

1 reference

2 August 2017

Catharina Schmidt

8

1 reference

2 August 2017

Elisabeth Ewers

9

1 reference

2 August 2017

Katharina Kreskowski

10

1 reference

2 August 2017

Monika Ziegler

11

1 reference

2 August 2017

Nadezda Kosyakova

12

1 reference

2 August 2017

Thomas Liehr

13

1 reference

2 August 2017

5 January 2011

1 reference

2 August 2017

Molecular Cytogenetics

1 reference

2 August 2017

4

1 reference

2 August 2017

1

1 reference

2 August 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1186/1755-8166-4-1

2 August 2017

0 references

cites work

Early embryonic chromosome instability results in stable mosaic pattern in human tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Amplification of 8q21 in breast cancer is independent of MYC and associated with poor patient outcome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Mechanisms of change in gene copy number

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

In vitro analysis of integrated global high-resolution DNA methylation profiling with genomic imbalance and gene expression in osteosarcoma

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Major changes in our DNA lead to major changes in our thinking

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Directly transmitted unbalanced chromosome abnormalities and euchromatic variants

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Detection of large-scale variation in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Large-scale copy number polymorphism in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

Overexpression, amplification, and androgen regulation of TPD52 in prostate cancer

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3024988

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21208402

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21208402

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8166-4-1

1 reference

Dimensions Publication ID

2 August 2017

1042114119

0 references

Fatcat ID

release_w5irwofq6vagdp7tlc6ancd3ia

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/w5irwofq6vagdp7tlc6ancd3ia

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

3024988

1 reference

2 August 2017

1 reference