(Q67993243)

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20 September 2019

title

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

1 reference

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20 September 2019

author name string

B. Dittrich

1

1 reference

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1 October 2022

W. P. Robinson

2

1 reference

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1 October 2022

H. Knoblauch

3

1 reference

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1 October 2022

K. Buiting

4

1 reference

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1 October 2022

K. Schmidt

5

1 reference

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1 October 2022

G. Gillessen-Kaesbach

6

1 reference

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1 October 2022

B. Horsthemke

7

1 reference

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1 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1487250

1 October 2022

publication date

1 November 1992

1 reference

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20 September 2019

1 reference

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20 September 2019

volume

90

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20 September 2019

issue

3

1 reference

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20 September 2019

page(s)

313-315

1 reference

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Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients

20 September 2019

cites work

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

The association of Angelman's syndrome with deletions within 15q11-13

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

Uniparental paternal disomy in Angelman's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1487250

12 December 2020

Identifiers

DOI

10.1007/BF00220089

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1487250%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

20 September 2019

1005722280

0 references

1 reference