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Beckwith-Wiedemann syndrome, tumourigenesis and imprinting
scientific article published on June 1992
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Beckwith-Wiedemann syndrome, tumourigenesis and imprinting
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
main subject
Beckwith-Wiedemann syndrome
1 reference
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inferred from title
author name string
Junien C
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
publication date
1 June 1992
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
published in
Current Opinion in Genetics & Development
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stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
volume
2
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stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
page(s)
431-438
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stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
cites work
Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Genomic imprinting in an Angelman and Prader-Willi translocation family
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Epigenetic control of transgene expression and imprinting by genotype-specific modifiers
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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A strain-specific modifier on mouse chromosome 4 controls the methylation of independent transgene loci
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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Genome imprinting and dominance modification
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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A new genetic concept: uniparental disomy and its potential effect, isodisomy
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Uniparental paternal disomy in a genetic cancer-predisposing syndrome
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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Isodisomy in BWS chromosomes
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Genomic imprinting, monozygous twinning, and X inactivation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Wiedemann-Beckwith syndrome in one of monozygotic twins
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Crossref
reference URL
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7 January 2021
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Monozygotic twinning and structural defects
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Wilms' tumour: reconciling genetics and biology
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Transcriptional repression mediated by the WT1 Wilms tumor gene product
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Familial predisposition to Wilms tumor does not segregate with the WT1 gene.
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of the mouse insulin-like growth factor II gene.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
based on heuristic
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Parental imprinting of the mouse H19 gene
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
1 reference
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Embryological and molecular investigations of parental imprinting on mouse chromosome 7.
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.
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7 January 2021
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Ectopic expression of the H19 gene in mice causes prenatal lethality
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Monoallelic expression of the human H19 gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Dads and disomy and disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of insulin-like growth factor-II transcripts in Wilms' tumour
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
based on heuristic
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Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
based on heuristic
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Tumour suppression associated with expression of human insulin-like growth factor II.
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https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
based on heuristic
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Three-generation dominant transmission of the Silver-Russell syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2805%2980154-6
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7 January 2021
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Identifiers
DOI
10.1016/S0959-437X(05)80154-6
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
PubMed ID
1504618
1 reference
stated in
Europe PubMed Central
PubMed ID
1504618
retrieved
9 August 2017
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