(Q33904998)

29 July 2017

title

Parental origin of chromosome 15 deletion in Prader-Willi syndrome (English)

1 reference

29 July 2017

main subject

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6134086

chromosomal deletion syndrome

11 August 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6134086

11 August 2023

0 references

M. G. Butler

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6134086

11 August 2023

language of work or name

English

0 references

publication date

1 June 1983

1 reference

29 July 2017

4 June 1983

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6134086

full work available at URL

11 August 2023

https://europepmc.org/articles/PMC5510872

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6134086

https://europepmc.org/articles/PMC5510872?pdf=render

11 August 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6134086

https://api.elsevier.com/content/article/PII:S0140-6736(83)92745-9?httpAccept=text/xml

11 August 2023

1 reference

10.1016/S0140-6736(83)92745-9

Crossref

DOI

https://api.crossref.org/works/10.1016/S0140-6736(83)92745-9

https://api.elsevier.com/content/article/PII:S0140-6736(83)92745-9?httpAccept=text/plain

11 August 2023

1 reference

10.1016/S0140-6736(83)92745-9

Crossref

DOI

https://api.crossref.org/works/10.1016/S0140-6736(83)92745-9

11 August 2023

1 reference

29 July 2017

1 reference

29 July 2017

issue

8336

1 reference

29 July 2017

page(s)

1285-1286

1 reference

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

29 July 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5510872

Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome

5 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5510872

On the structure and polymorphism of the human chromosome no. 15

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6134086

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6134086

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6134086

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0140-6736(83)92745-9

1 reference

29 July 2017

1 reference

29 July 2017

1 reference