(Q48168107)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

title

Atypical Prader-Willi syndrome with severe developmental delay and emaciation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

main subject

Prader–Willi syndrome

1 reference

T Miike

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

T Ogata

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

Y Ohtani

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

H Yamaguchi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

Y Yokoyama

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

publication date

1 January 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

published in

Brain and Development

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

page(s)

186-188

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases

29 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980026-3

7 January 2021

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980026-3

7 January 2021

The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980026-3

7 January 2021

Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980026-3

7 January 2021

Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980026-3

7 January 2021

10.1016/S0387-7604(88)80026-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2457332%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

1 reference