(Q72797465)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

Beckwith-Wiedemann syndrome

29 October 2019

main subject

1 reference

A Nyström

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

F Hedborg

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

R Ohlsson

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

publication date

1 August 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

29 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

153

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

page(s)

574-580

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf02190661

29 October 2019

exact match

0 references

cites work

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

1 reference

12 December 2020

Relaxation of imprinted genes in human cancer.

1 reference

12 December 2020

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

1 reference

12 December 2020

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

1 reference

12 December 2020

Neurodevelopmental outcome of asymptomatic & symptomatic babies with neonatal hypoglycaemia.

1 reference

12 December 2020

Neurological findings at follow-up in neonatal hypoglycaemia

1 reference

12 December 2020

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

12 December 2020

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

1 reference

12 December 2020

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

12 December 2020

Insulin-like growth factors I and II.

1 reference

12 December 2020

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

12 December 2020

Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases

1 reference

12 December 2020

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

1 reference

12 December 2020

Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases

1 reference

12 December 2020

Insulin-like growth factor 2 and short-range stimulatory loops in control of human placental growth

1 reference

12 December 2020

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

1 reference

12 December 2020

Genomic imprinting and the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

1 reference

12 December 2020

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

12 December 2020

Bronze baby syndrome, biliary hypoplasia, incomplete Beckwith-Wiedemann syndrome and partial trisomy 11

1 reference

12 December 2020

The "E.M.G." syndrome (Exomphalos, Macroglossia, Gigantism).

1 reference

12 December 2020

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1 reference

12 December 2020

Dominant inheritance of Wiedemann-Beckwith syndrome: further evidence for transmission of "unstable premutation" through carrier women

1 reference

12 December 2020

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02190661

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7957404%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference