(Q55026497)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

title

Anthropometric study with emphasis on hand and foot measurements in the Prader-Willi syndrome: sex, age and chromosome effects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

main subject

Prader–Willi syndrome

1 reference

M G Butler

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

J L Haynes

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

F J Meaney

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

publication date

1 January 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

volume

39

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

page(s)

39-47

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

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

22 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feet

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Prader-Willi syndrome: current understanding of cause and diagnosis

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Craniofacial variation and growth in the Prader-Labhart-Willi syndrome.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Neonatal diagnosis of Prader-Willi syndrome and its implications

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5985666

Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population

13 August 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion

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

Normal values for selected physical parameters: an aid to syndrome delineation

1 reference

12 December 2020

10.1111/J.1399-0004.1991.TB02983.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1997214%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

PubMed publication ID

1997214

1 reference