(Q35716500)

9 August 2017

1 reference

title

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting (English)

1 reference

Beckwith-Wiedemann syndrome

9 August 2017

main subject

1 reference

Junien C

1 reference

9 August 2017

publication date

1 June 1992

1 reference

Current Opinion in Genetics & Development

9 August 2017

published in

1 reference

9 August 2017

1 reference

9 August 2017

1 reference

9 August 2017

page(s)

431-438

1 reference

Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas

9 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Genomic imprinting in an Angelman and Prader-Willi translocation family

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Epigenetic control of transgene expression and imprinting by genotype-specific modifiers

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

A strain-specific modifier on mouse chromosome 4 controls the methylation of independent transgene loci

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Genome imprinting and dominance modification

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

A new genetic concept: uniparental disomy and its potential effect, isodisomy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Isodisomy in BWS chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Genomic imprinting, monozygous twinning, and X inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Wiedemann-Beckwith syndrome in one of monozygotic twins

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Monozygotic twinning and structural defects

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Wilms' tumour: reconciling genetics and biology

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Transcriptional repression mediated by the WT1 Wilms tumor gene product

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Familial predisposition to Wilms tumor does not segregate with the WT1 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Ectopic expression of the H19 gene in mice causes prenatal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Dads and disomy and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Expression of insulin-like growth factor-II transcripts in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Tumour suppression associated with expression of human insulin-like growth factor II.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

Three-generation dominant transmission of the Silver-Russell syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6

7 January 2021

10.1016/S0959-437X(05)80154-6

Identifiers

DOI

1 reference

9 August 2017

1 reference