(Q72802890)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

main subject

Prader–Willi syndrome

1 reference

B Dittrich

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

K Buiting

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

S Gross

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

B Horsthemke

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

publication date

1 November 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

94

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

page(s)

583-584

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00211036

29 October 2019

exact match

0 references

cites work

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

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

1 reference

12 December 2020

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

1 reference

12 December 2020

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

12 December 2020

Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene

1 reference

12 December 2020

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

1 reference

12 December 2020

An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13

1 reference

12 December 2020

Linkage analysis in familial Angelman syndrome

1 reference

12 December 2020

Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

1 reference

12 December 2020

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

1 reference

12 December 2020

Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications

1 reference

12 December 2020

Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00211036

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7959704%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference