(Q35602615)

9 August 2017

Wiedemann-Beckwith syndrome in one of monozygotic twins (English)

1 reference

9 August 2017

Bose B

1

1 reference

9 August 2017

Wilkie RA

2

1 reference

9 August 2017

Madlom M

3

1 reference

9 August 2017

Forsyth JS

4

1 reference

9 August 2017

Faed MJ

5

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 December 1985

1 reference

Archives of Disease in Childhood

9 August 2017

1 reference

9 August 2017

60

1 reference

9 August 2017

1191-1192

1 reference

9 August 2017

12

1 reference

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

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777666

Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777666

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777666

Monozygotic twinning and structural defects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1777666

The Beckwith-Wiedmann syndrome

12 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4091589

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Localization of insulin-like growth factor genes to human chromosomes 11 and 12

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4091589

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.60.12.1191

1 reference

9 August 2017

1 reference

9 August 2017

1 reference