(Q28208127)

inferred from title

Prader–Willi syndrome

1 reference

T Ozçelik

1

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S Leff

2

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W Robinson

3

0 references

T Donlon

4

0 references

M Lalande

5

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E Sanjines

6

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A Schinzel

7

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U Francke

Monoallelic expression of the human H19 gene

8

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language of work or name

English

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publication date

December 1992

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published in

Nature Genetics

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volume

2

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issue

4

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page(s)

265-9

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG1292-265

Parental imprinting of the mouse H19 gene

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1292-265

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

Uniparental paternal disomy in Angelman's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

Regulated expression of the small nuclear ribonucleoprotein particle protein SmN in embryonic stem cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Prader-Willi syndrome: current understanding of cause and diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

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%2FNG1292-265

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Messenger RNA Splicing in Yeast: Clues to Why the Spliceosome Is a Ribonucleoprotein

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypeptide N.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Isolation of cDNA clones encoding small nuclear ribonucleoparticle-associated proteins with different tissue specificities

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

A comparison of snRNP-associated Sm-autoantigens: human N, rat N and human B/B'

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Genes for beta 2-adrenergic receptor and platelet-derived growth factor receptor map to mouse chromosome 18

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

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%2FNG1292-265

7 January 2021

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

DNA deletion and its parental origin in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Regional assignment of genes for mannose phosphate isomerase, pyruvate kinase-3, and beta 2-microglobulin expression on human chromosome 15 by hybridization of cells from a t(15;22) (q14;q13.3) translocation carrier.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

Assignment of the major histocompatibility complex to a region of the short arm of human chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-265

7 January 2021

release_b634ej4o5bbw7mtpv6nhnjzope

Identifiers

DOI

10.1038/NG1292-265

0 references

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/b634ej4o5bbw7mtpv6nhnjzope

24 November 2022