(Q33667858)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

title

Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

A C Berry

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

E M Belton

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

C Chantler

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

language of work or name

English

0 references

publication date

1 April 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

12 October 2019

published in

1 reference

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12 October 2019

volume

1 reference

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12 October 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

page(s)

136-138

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?

12 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048520

Exomphalos with macroglossia: a study of eleven cases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048520

The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048520

Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048520

Letter: Wiedemann-Beckwith 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=1048520

The Beckwith-Wiedmann syndrome

21 June 2018

1 reference

12 December 2020

The Beckwith-Wiedemann syndrome. Seven new cases

1 reference

12 December 2020

Wiedemann-Beckwith syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Letter: Pseudo-Beckwith-Wiedemann syndrome: interaction with maternal diabetes

1 reference

12 December 2020

Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome

1 reference

12 December 2020

Beckwith-Wiedemann syndrome in a mother and her son

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.17.2.136

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

PubMed publication ID

7189783

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7189783%20AND%20SRC:MED&resulttype=core&format=json