(Q37624720)

21 August 2017

Methylation PCR analysis of Prader-Willi syndrome, Angelman syndrome, and control subjects (English)

1 reference

21 August 2017

1 reference

Prader–Willi syndrome

1 reference

B Muralidhar

1

1 reference

PMC publication ID

5292048

21 August 2017

M G Butler

series ordinal

2

1 reference

21 August 2017

1 November 1998

1 reference

American Journal of Medical Genetics Part A

21 August 2017

1 reference

21 August 2017

80

1 reference

21 August 2017

3

1 reference

21 August 2017

263-265

1 reference

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

21 August 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5292048

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

23 August 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5292048

Methylation-specific PCR simplifies imprinting analysis

23 August 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5292048

Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome

25 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9843050

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/(SICI)1096-8628(19981116)80:3<263::AID-AJMG16>3.3.CO;2-7

1 reference

21 August 2017

1 reference

PMC publication ID

5292048

21 August 2017

PubMed publication ID

9843050

1 reference

PMC publication ID

5292048