(Q68330563)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

chromosomal deletion syndrome

23 September 2019

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

nucleic acid sequence homology

28 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

J. R. Chaillet

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

J. H. Knoll

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

B. Horsthemke

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

M. Lalande

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1685485

28 October 2022

publication date

1 November 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

23 September 2019

https://api.elsevier.com/content/article/PII:0888754391900902?httpAccept=text/xml

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

https://api.elsevier.com/content/article/PII:0888754391900902?httpAccept=text/plain

28 October 2022

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

page(s)

773-776

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences

23 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

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

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Is Angelman syndrome an alternate result of del(15)(q11q13)?

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2.

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Genetic variation at a locus (TAM-1) for submaxillary gland protease in the mouse and its location on chromosome No. 7

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Differential imprinting and expression of maternal and paternal genomes

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

28 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json