(Q40810626)

English

A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms.

scientific article published on May 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Martin Hergersberg

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Baumer A

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Wiedemann U

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Schinzel A

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 May 2001

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

17

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

423-430

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1118

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.1118

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11317358%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

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