(Q52007443)

19 April 2018

title

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

1 reference

19 April 2018

main subject

Prader–Willi syndrome

1 reference

Joyce E Whittington

1

1 reference

19 April 2018

Jill V Butler

series ordinal

2

1 reference

19 April 2018

Anthony J Holland

series ordinal

3

1 reference

19 April 2018

publication date

6 September 2006

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19 April 2018

European Journal of Human Genetics

published in

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19 April 2018

volume

15

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19 April 2018

issue

1

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19 April 2018

page(s)

127-130

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19 April 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

Birth prevalence of Prader-Willi syndrome in Australia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

Biological aging and the etiology of aneuploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

Risk factors for nondisjunction of trisomy 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

Genomic imprinting as a cause of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

Relationship between clinical and genetic diagnosis of Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

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%2FSJ.EJHG.5201716

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

Parental exposure to hydrocarbons in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

inferred from DOI database lookup

7 January 2021

based on heuristic

Cytogenetic and age-dependent risk factors associated with uniparental disomy 15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201716

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201716

1 reference

19 April 2018

1 reference

19 April 2018