(Q81596609)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

Frequency of new copy number variation in humans (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Gert-Jan B van Ommen

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

publication date

1 April 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

volume

37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

page(s)

333-334

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0405-333

10 January 2020

exact match

0 references

cites work

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Recent segmental duplications in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Shotgun sequence assembly and recent segmental duplications within the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

The rate of spontaneous mutation of a human gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0405-333

7 January 2021

Identifiers

DOI

10.1038/NG0405-333

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15800641%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference