(Q33244469)

24 July 2017

Uniparental paternal disomy in Angelman's syndrome (English)

1 reference

chromosomal deletion syndrome

24 July 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

genomic library

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

6

J. A. Armour

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

author name string

S. Malcolm

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

J. Clayton-Smith

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

M. Nichols

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

S. Robb

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

T. Webb

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

A. J. Jeffreys

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

M. E. Pembrey

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1672177

25 October 2022

language of work or name

English

0 references

publication date

1 March 1991

1 reference

24 July 2017

23 March 1991

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1672177

full work available at URL

25 October 2022

https://api.elsevier.com/content/article/PII:014067369190278W?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

https://api.elsevier.com/content/article/PII:014067369190278W?httpAccept=text/plain

25 October 2022

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

25 October 2022

1 reference

24 July 2017

337

1 reference

24 July 2017

694-697

1 reference

24 July 2017

8743

1 reference

Differential activity of maternally and paternally derived chromosome regions in mice

24 July 2017

1

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

‘Puppet’ Children A Report on Three Cases

25 October 2022

2

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

The EEG in early diagnosis of the Angelman (happy puppet) syndrome.

25 October 2022

3

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

25 October 2022

4

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

The association of Angelman's syndrome with deletions within 15q11-13

25 October 2022

5

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

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

25 October 2022

6

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

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

25 October 2022

7

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons

25 October 2022

8

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

25 October 2022

9

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Cytogenetic and molecular study of Angelman syndrome

25 October 2022

10

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

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

25 October 2022

11

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Prader-Willi syndrome: current understanding of cause and diagnosis

25 October 2022

12

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

25 October 2022

14

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

On the parental origin of the deletion in Angelman syndrome

25 October 2022

15

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

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

25 October 2022

16

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Systematic cloning of human minisatellites from ordered array charomid libraries.

25 October 2022

18

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24].

25 October 2022

19

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

A mapped set of DNA markers for human chromosome 15.

25 October 2022

20

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

25 October 2022

21

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

A new genetic concept: uniparental disomy and its potential effect, isodisomy

25 October 2022

23

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)90278-W

25 October 2022

Identifiers

1 reference

24 July 2017

1 reference