Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness Patterning (Q37300984)

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scientific article published on September 1989

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Language	Label	Description	Also known as
English	Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness Patterning	scientific article published on September 1989

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

title

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

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

main subject

obesity

0 references

author name string

F John Meaney

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

Merlin G Butler

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

language of work or name

English

1 reference

based on heuristic

inferred from title

publication date

1 September 1989

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

published in

Medical Anthropology Quarterly

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

volume

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

issue

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

page(s)

294-305

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

Skinfolds and body density and their relation to body fatness: a review

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

An anthropometric study of 38 individuals with Prader-Labhart-Willi syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

Revised standards for triceps and subscapular skinfolds in British children

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

6 September 2017

Clinical anthropometry and medical genetics: a compilation of body measurements in genetic and congenital disorders

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

14 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

14 September 2017

Weight control of children with Prader-Willi syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

26 June 2018

Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

26 June 2018

Skinfold equations for estimation of body fatness in children and youth.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

26 June 2018

The developing role of anthropologists in medical genetics: anthropometric assessment of the Prader-Labhart-Willi syndrome as an illustration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

26 June 2018

NCHS growth curves for children birth-18 years. United States

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

26 June 2018

HYPOGENITAL DYSTROPHY WITH DIABETIC TENDENCY

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

2 September 2018

Generalized equations for predicting body density of women.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

2 September 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5045040

retrieved

2 September 2018

Skinfolds, body girths, biacromial diameter, and selected anthropometric indices of adults. United States, 1960-1962

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/27695159

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of skinfold measurements to judge obesity during the early phase of Prader-Labhart-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/27695159

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid metabolic disturbances in Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/27695159

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Food and children with Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/27695159

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1525/MAQ.1989.3.3.02A00080

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

PMC publication ID

5045040

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

PubMed publication ID

27695159

1 reference

stated in

Europe PubMed Central

PMC publication ID

5045040

retrieved

19 August 2017

 

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