(Q45399577)

14 December 2017

title

The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea (English)

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14 December 2017

main subject

Prader–Willi syndrome

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2

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14 December 2017

Sung Yoon Cho

1

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14 December 2017

Young Bae Sohn

3

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14 December 2017

Se Hyun Maeng

4

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14 December 2017

You Jin Jung

5

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14 December 2017

Su Jin Kim

6

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14 December 2017

Dong-Kyu Jin

7

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14 December 2017

publication date

10 January 2013

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Journal of Human Genetics

14 December 2017

published in

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14 December 2017

volume

58

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14 December 2017

issue

3

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14 December 2017

page(s)

150-154

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https://scigraph.springernature.com/pub.10.1038/jhg.2012.148

14 December 2017

exact match

0 references

cites work

Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

21 January 2018

Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

The Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Sleep and breathing in patients with the Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Methylation-specific PCR simplifies imprinting analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Understanding the impact of 1q21.1 copy number variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Biological aging and the etiology of aneuploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Risk factors for nondisjunction of trisomy 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

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.2012.148

7 January 2021

Parental exposure to hydrocarbons in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

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.2012.148

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.148

7 January 2021

Identifiers

DOI

10.1038/JHG.2012.148

1 reference

Dimensions Publication ID

14 December 2017

1047578636

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1 reference