Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats (Q48050604)

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scientific article published in May 1997

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Language	Label	Description	Also known as
English	Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats	scientific article published in May 1997

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

title

Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

author name string

Small K

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

Iber J

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

Warren ST

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

language of work or name

English

0 references

publication date

1 May 1997

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

published in

Nature Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

volume

16

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

page(s)

96-99

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

cites work

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

The exon-intron organization of the human X-linked gene (FLN1) encoding actin-binding protein 280.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

Mechanisms of nonhomologous recombination in mammalian cells

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

Integration of gene maps: chromosome X

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

21 January 2018

Emery-Dreifuss syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Nonhomologous recombination in the human genome: deletions in the human factor VIII gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Actin-binding protein requirement for cortical stability and efficient locomotion

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular characterization of a pericentric inversion in mouse chromosome 8 implicates telomeres as promoters of meiotic recombination

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A dual level model for speciation by multiple pericentric inversions.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A YAC clone map spanning 7.5 megabases of human chromosome band Xq28.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

G6PD haplotypes spanning Xq28 from F8C to red/green color vision

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A muscle-specific DNase I-like gene in human Xq28.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0597-96

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG0597-96

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

PubMed publication ID

9140403

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9140403

retrieved

8 February 2018

reference URL

http://europepmc.org/abstract/MED/9140403

ResearchGate publication ID

14078834

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