Problems in detecting mosaic DNA methylation in Angelman syndrome (Q79108261)

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19 December 2019

title

Problems in detecting mosaic DNA methylation in Angelman syndrome (English)

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19 December 2019

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24

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19 December 2019

10

Elke Holinski-Feder

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19 December 2019

16

Peter Kroisel

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19 December 2019

12

Stephanie Kleinle

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19 December 2019

author name string

Bernhard Horsthemke

1

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19 December 2019

Christina Lich

2

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19 December 2019

Karin Buiting

3

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19 December 2019

Roland Achmann

4

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19 December 2019

Christa Aulehla-Scholz

5

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19 December 2019

Alessandra Baumer

6

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19 December 2019

Joachim Bürger

7

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19 December 2019

Bernd Dworniczak

8

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19 December 2019

Dieter Gläser

9

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19 December 2019

Bart Janssen

11

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19 December 2019

Lothar Kochhan

13

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19 December 2019

Ernst Krasemann

14

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19 December 2019

Cornelia Kraus

15

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19 December 2019

Hansjörg Plendl

17

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19 December 2019

Sabine Purmann

18

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19 December 2019

Gabriele Sander

19

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19 December 2019

Heyko Skladny

20

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19 December 2019

Eva Spitzer

21

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19 December 2019

Barbara Thamm-Mücke

22

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19 December 2019

Raymonda Varon-Mateeva

23

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19 December 2019

Helga Weirich

25

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19 December 2019

publication date

1 December 2003

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European Journal of Human Genetics

19 December 2019

published in

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19 December 2019

volume

11

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19 December 2019

issue

12

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19 December 2019

page(s)

913-915

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Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

19 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201078

7 January 2021

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/10.1038%2FSJ.EJHG.5201078

7 January 2021

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201078

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%2FSJ.EJHG.5201078

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201078

7 January 2021

A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201078

7 January 2021

A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201078

7 January 2021

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201078

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201078

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19 December 2019

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