(Q34329545)

1 August 2017

title

Different distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly (English)

1 reference

1 August 2017

main subject

Prader–Willi syndrome

1 reference

Margje Sinnema

1

1 reference

1 August 2017

Kees E P van Roozendaal

2

1 reference

1 August 2017

Marian A Maaskant

3

1 reference

1 August 2017

Hubert J M Smeets

4

1 reference

1 August 2017

John J M Engelen

5

1 reference

1 August 2017

Nieke Jonker-Houben

6

1 reference

1 August 2017

Constance T R M Schrander-Stumpel

7

1 reference

1 August 2017

Leopold M G Curfs

8

1 reference

1 August 2017

publication date

12 May 2010

1 reference

European Journal of Human Genetics

1 August 2017

published in

1 reference

1 August 2017

volume

18

1 reference

1 August 2017

issue

9

1 reference

1 August 2017

page(s)

993-998

1 reference

Does assisted reproductive technology cause birth defects?

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Imprinting disorders and assisted reproductive technology

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Recommendations for the diagnosis and management of Prader-Willi syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

A Systematic Review of Mortality in Schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Neural mechanisms underlying hyperphagia in Prader-Willi syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Mortality in Prader-Willi syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Birth prevalence of Prader-Willi syndrome in Australia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Possible dosage effect of maternally expressed genes on visual recognition memory in Prader-Willi syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

6 July 2018

Prader-Willi syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Prader-Willi syndrome: consensus diagnostic criteria.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

6 July 2018

Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Prader-Willi syndrome: causes of death in an international series of 27 cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Death in adults with Prader-Willi syndrome may be correlated with maternal uniparental disomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Psychotic disorders in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987424

Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20461108

12 December 2020

inferred from PubMed ID database lookup

Parental exposure to hydrocarbons in Prader-Willi syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20461108

12 December 2020

inferred from PubMed ID database lookup

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20461108

12 December 2020

inferred from PubMed ID database lookup

Possible dosage effect of maternally expressed genes on visual recognition memory in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.67

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/EJHG.2010.67

1 reference

1 August 2017

1 reference

1 August 2017

1 reference