(Q84246759)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

Maternal age effect on the development of Prader-Willi syndrome resulting from upd(15)mat through meiosis 1 errors (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

main subject

Prader–Willi syndrome

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

author name string

Keiko Matsubara

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Nobuyuki Murakami

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Toshiro Nagai

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

publication date

2 June 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

2 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

566-571

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/jhg.2011.59

2 February 2020

exact match

0 references

cites work

Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

American College of Medical Genetics statement of diagnostic testing for uniparental disomy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Meiosis in oocytes: predisposition to aneuploidy and its increased incidence with age.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

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%2FJHG.2011.59

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Mechanisms leading to uniparental disomy and their clinical consequences

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Advanced parental age in maternal uniparental disomy (UPD): implications for the mechanism of formation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

New insights into human nondisjunction of chromosome 21 in oocytes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Effects of male age on the frequencies of germinal and heritable chromosomal abnormalities in humans and rodents

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Gender effects on the incidence of aneuploidy in mammalian germ cells

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Paternal hydrocarbon exposure in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Parental exposure to hydrocarbons in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

The occurrence of aneuploidy in human: lessons from the cytogenetic studies of human oocytes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.59

7 January 2021

Identifiers

DOI

10.1038/JHG.2011.59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21633360%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference