(Q26775039)

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Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

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Thomas Liehr

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publication date

22 January 2016

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

Molecular Cytogenetics

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

9

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1

0 references

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

The great human expansion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

7 April 2017

Practical issues in screening and variable selection in genome-wide association analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

7 April 2017

Detection of large-scale variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

7 April 2017

Large-scale copy number polymorphism in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

7 April 2017

Our Fragile Intellect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

7 April 2017

Heteromorphic variants of chromosome 9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

The human genome puzzle - the role of copy number variation in somatic mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

The pursuit of genome-wide association studies: where are we now?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

Human interphase chromosomes: a review of available molecular cytogenetic technologies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

Recent development in pharmacogenomics: from candidate genes to genome-wide association studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

SNPs in forensic genetics: a review on SNP typing methodologies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

Directly transmitted unbalanced chromosome abnormalities and euchromatic variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

Copy-number polymorphisms: mining the tip of an iceberg

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

Transcriptional activation of a constitutive heterochromatic domain of the human genome in response to heat shock.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

Aging, evolution and individual health span: introduction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 September 2017

An eleven-generation satellited Y chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

31 May 2018

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-016-0216-1

21 January 2018

A survey of a familial transmission of an anomalous autosome in group 13-15.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-016-0216-1

21 January 2018

Genetic entropy and the human intellect.

1 reference

https://api.crossref.org/works/10.1186%2FS13039-016-0216-1

21 January 2018

Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724132

28 November 2018

Distribution of the D15Z1 copy number polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/26807150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The sites and relative frequencies of secondary constrictions in human somatic chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/26807150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid prenatal diagnostics in the interphase nucleus: procedure and cut-off rates

1 reference

https://pubmed.ncbi.nlm.nih.gov/26807150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enlarged chromosome 13 p‐arm hiding a cryptic partial trisomy 6p22.2‐pter

1 reference

https://pubmed.ncbi.nlm.nih.gov/26807150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Our fragile intellect: response to Dr Mitchell

1 reference

https://pubmed.ncbi.nlm.nih.gov/26807150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spurious monosomy 7 in leukemia due to centromeric heteromorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/26807150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/S13039-016-0216-1

2 references

Consolidated OpenCitations Corpus – April 2017

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26807150%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

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