(Q40286845)

English

Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin

scientific article published on 20 September 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

0 references

author name string

Lionel R Willatt

1

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

John C K Barber

2

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Amanda Clarkson

3

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Ingrid Simonic

4

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

F Lucy Raymond

5

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Zoe Docherty

6

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Caroline Mackie Ogilvie

7

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

publication date

20 September 2006

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

15

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

45-52

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201720

0 references

Recent duplication, domain accretion and the dynamic mutation of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Segmental duplications and copy-number variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

DNA sequence and analysis of human chromosome 9

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Directly transmitted unbalanced chromosome abnormalities and euchromatic variants

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Euchromatic 9q + heteromorphism in a family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Del(3) (p25.3) without phenotypic effect

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Variants of chromosome 9 with additional euchromatic bands: two case reports

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Genomic structure and evolution of the ancestral chromosome fusion site in 2q13-2q14.1 and paralogous regions on other human chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

An assessment of the sequence gaps: unfinished business in a finished human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Lessons from the human genome: transitions between euchromatin and heterochromatin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

The structure and evolution of centromeric transition regions within the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

21 January 2018

Human chromosome 9 pericentric homologies: implications for chromosome 9 heteromorphisms.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

A G-band study of chromosomes in liveborn infants

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

An extra band in human 9qh+ chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

Extra euchromatic band in the qh region of chromosome 9

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

Rare variant of chromosome 9

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201720

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201720

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

ResearchGate publication ID

0 references

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