(Q67510275)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference

Wagstaff J

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Knoll JH

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Glatt KA

3

1 reference

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14 September 2019

Shugart YY

4

1 reference

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14 September 2019

Sommer A

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Lalande M

6

1 reference

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14 September 2019

publication date

1 July 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

number of pages

4

1 reference

inferred from page(s)

published in

Nature Genetics

1 reference

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14 September 2019

volume

1

1 reference

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14 September 2019

issue

4

1 reference

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14 September 2019

page(s)

291-294

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

‘Puppet’ Children A Report on Three Cases

14 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Deletions of proximal 15q without Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Genomic imprinting in an Angelman and Prader-Willi translocation family

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

DNA deletion and its parental origin in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

The Angelman (Happy Puppet) syndrome: is it autosomal recessive?

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0792-291

7 January 2021

Identifiers

DOI

10.1038/NG0792-291

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1338769%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference