(Q33594824)

28 July 2017

title

The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes (English)

1 reference

28 July 2017

Hughes-Benzie R

1

1 reference

28 July 2017

R. Hughes-Benzie

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1479609

30 September 2022

J. Allanson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1479609

30 September 2022

A. Hunter

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1479609

30 September 2022

T. Cole

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1479609

30 September 2022

language of work or name

English

0 references

publication date

1 December 1992

1 reference

full work available at URL

28 July 2017

https://europepmc.org/articles/PMC1016224

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1479609

https://europepmc.org/articles/PMC1016224?pdf=render

30 September 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1479609

Journal of Medical Genetics

30 September 2022

published in

1 reference

28 July 2017

volume

29

1 reference

28 July 2017

issue

12

1 reference

28 July 2017

page(s)

928

1 reference

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016224

Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016224

Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016224

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016224

The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1479609

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Monozygotic twinning and Wiedemann-Beckwith syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1479609

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.29.12.928-B

1 reference

28 July 2017

1 reference

28 July 2017

1 reference