(Q57976812)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

Beckwith-Wiedemann syndrome

15 January 2020

main subject

1 reference

based on heuristic

inferred from title

Silver-Russell syndrome

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Maria Vittoria Cubellis

6

1 reference

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15 January 2020

Andrea Riccio

11

1 reference

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15 January 2020

author name string

Laura Cardarelli

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Agostina De Crescenzo

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Elisa Nalesso

4

1 reference

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15 January 2020

Angelo Selicorni

7

1 reference

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15 January 2020

Paola Cavicchioli

8

1 reference

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15 January 2020

Giovanni Battista Pozzan

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Marilena Petrella

10

1 reference

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15 January 2020

Barbara Zavan

5

1 reference

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15 January 2020

publication date

1 July 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

Pediatric and Developmental Pathology

15 January 2020

published in

1 reference

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15 January 2020

volume

13

1 reference

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15 January 2020

issue

4

1 reference

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15 January 2020

page(s)

326-330

1 reference

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Genomic imprinting: parental influence on the genome

15 January 2020

cites work

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regions.

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F09-07-0686-CR.1

21 January 2018

Identifiers

DOI

10.2350/09-07-0686-CR.1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20028213%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference