(Q37229655)

19 August 2017

Prader-Willi Syndrome: Genetics and Behavior (English)

1 reference

19 August 2017

Prader–Willi syndrome

1 reference

Travis Thompson

1

1 reference

19 August 2017

Merlin G Butler

series ordinal

2

1 reference

19 August 2017

William E MacLean

series ordinal

3

1 reference

19 August 2017

Beth Joseph

series ordinal

4

1 reference

19 August 2017

1 January 1996

1 reference

Peabody Journal of Education

19 August 2017

1 reference

19 August 2017

71

1 reference

19 August 2017

4

1 reference

19 August 2017

187-212

1 reference

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

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Preventing mental retardation associated with gross obesity in the Prader-Willi syndrome.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Conditional discrimination vs. matching to sample: an expansion of the testing paradigm

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

The Prader-Willi syndrome: a study of 40 patients and a review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Prader-Willi syndrome: current understanding of cause and diagnosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Issues in the classification of mental retardation: differentiating among organic etiologies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

The Prader-Labhart-Willi syndrome: review of the literature and report of nine cases

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

The repeated acquisition of behavioral chains

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Food- and nonfood-related differential outcomes in equivalence learning by adults with Prader-Willi syndrome.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation)

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Emotional symptoms in Prader-Willi syndrome adolescents.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

The speech and language characteristics of children with Prader-Willi syndrome.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Profiles, correlates, and trajectories of intelligence in Prader-Willi syndrome

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

‘Puppet’ Children A Report on Three Cases

26 June 2018

1 reference

https://api.crossref.org/works/10.1080%2F01619569609595137

Personality profiles of youngsters with Prader‐Willi syndrome and youngsters attending regular schools

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F01619569609595137

Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness Patterning

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F01619569609595137

Obsessions and compulsions in Prader-Willi syndrome.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Behavioral and emotional problems in youngsters with Prader-Willi syndrome

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Are expectancies based upon different positive reinforcing events discriminably different?

3 September 2018

1 reference

https://api.crossref.org/works/10.1080%2F01619569609595137

A survey of the phenomenology and pharmacotherapy of compulsive and impulsive-aggressive symptoms in Prader-Willi syndrome

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5010090

Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome

20 October 2018

1 reference

12 December 2020

RESTING METABOLIC RATE IN PRADER-WILLI SYNDROME

1 reference

12 December 2020

Paternal hydrocarbon exposure in Prader-Willi syndrome

1 reference

12 December 2020

Energy expenditure and body composition in Prader-Willi syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Neuropsychological capacity of Prader-Willi children: general and specific aspects of impairment

1 reference

12 December 2020

Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence

1 reference

12 December 2020

Prader-Willi syndrome

1 reference

12 December 2020

Cytogenetic and molecular analysis in Angelman syndrome

1 reference

12 December 2020

10.1080/01619569609595137

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

27594721

1 reference