(Q42538525)

1 November 2017

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The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish population (English)

1 reference

1 November 2017

Silverstein S

1

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1 November 2017

Lerer I

series ordinal

2

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1 November 2017

Buiting K

series ordinal

3

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1 November 2017

Abeliovich D

series ordinal

4

1 reference

1 November 2017

language of work or name

English

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publication date

17 November 2000

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American Journal of Human Genetics

1 November 2017

1 reference

1 November 2017

68

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1 November 2017

1

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1 November 2017

261-263

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A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?

1 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1234924

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1234924

Imprinting in Prader-Willi and Angelman syndromes.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1234924

Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR method

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1234924

DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting

16 August 2018

1 reference

12 December 2020

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

1 reference

12 December 2020

Molecular diagnosis of Prader-Willi syndrome: parent-of-origin dependent methylation sites and non-isotopic detection of (CA)n dinucleotide repeat polymorphisms

1 reference

12 December 2020

Diagnostic testing for Prader-Willi and Angleman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee

1 reference

12 December 2020

A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus

1 reference

12 December 2020

Identifiers

DOI

10.1086/316943

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1 November 2017

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1 November 2017

1 reference