(Q51893780)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

main subject

Prader–Willi syndrome

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

author name string

G B Peters

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

J M Carmichael

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

A P Darmanian

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

F A Collins

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

publication date

13 February 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

volume

73

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

page(s)

353-359

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.

2 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00960.X

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00960.X

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2007.00960.X

10.1111/J.1399-0004.2007.00960.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18279435%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference