(Q52170199)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

main subject

Prader–Willi syndrome

1 reference

4

I D Feurer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

E Roof

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

W Stone

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

W MacLean

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

T Thompson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

M G Butler

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

publication date

1 February 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

Journal of Intellectual Disability Research

4 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

44 ( Pt 1)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

25-30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

Prader-Willi syndrome: current understanding of cause and diagnosis

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Prader-Willi syndrome and psychotic symptoms: 2. A preliminary study of prevalence using the Psychopathology Assessment Schedule for Adults with Developmental Disability checklist.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Adults with Prader-Willi syndrome: abnormalities of sleep and behaviour.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Obsessions and compulsions in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Families of children with Prader-Willi syndrome: stress-support and relations to child characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Self-injurious behavior and Prader-Willi syndrome: behavioral forms and body locations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Prader-Willi syndrome and cycloid psychoses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2788.2000.00250.X

Obsessive-compulsive disorder in mentally retarded patients.

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Estimation of human body composition by electrical impedance methods: a comparative study.

1 reference

12 December 2020

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.

1 reference

12 December 2020

Prader-Willi Syndrome: Genetics and Behavior

1 reference

12 December 2020

Prader-Willi syndrome

1 reference

12 December 2020

Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings.

1 reference

12 December 2020

Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome

1 reference

12 December 2020

Adults with Prader-Willi syndrome: a survey of 232 cases

1 reference

12 December 2020

Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

1 reference

12 December 2020

Adaptive and maladaptive behavior in Prader-Willi syndrome

1 reference

12 December 2020

Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies

1 reference

12 December 2020

Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15

1 reference

12 December 2020

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele

1 reference

12 December 2020

Dual-energy x-ray absorptiometry for total-body and regional bone-mineral and soft-tissue composition

1 reference

12 December 2020

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

1 reference

12 December 2020

10.1046/J.1365-2788.2000.00250.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10711647%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

PubMed publication ID

10711647

1 reference