Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry
about
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromeBeckwith-Wiedemann syndrome and IVF: a case-control studyAssociation of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defectsGenetic and nongenetic risk factors for childhood cancerSilver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular EtiologyThe epidemiology of hepatoblastomaA Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.ChIPseek, a web-based analysis tool for ChIP dataBirth characteristics and the risk of childhood rhabdomyosarcoma based on histological subtype.Genetic syndromes associated with overgrowth in childhood.Recognition and management of childhood cancer syndromes: a systems approach.Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects.Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumorFive additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocol.Beckwith-Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same geneChest wall hamartoma with Wiedemann-Beckwith syndrome: clinical report and brief review of chromosome 11p15.5-related tumors.Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cellsAssociation between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsRole of liver transplantation in the management of hepatoblastoma in the pediatric population.Ovarian thecal metaplasia of the adrenal gland in association with Beckwith-Wiedemann syndrome.Genetic alterations in hepatoblastoma and hepatocellular carcinoma: common and distinctive aspects.Pathology from evolutionary conflict, with a theory of X chromosome versus autosome conflict over sexually antagonistic traits.Clonality and evolutionary history of rhabdomyosarcomaBeckwith-Wiedemann syndrome and isolated hemihyperplasia.Infant Cancer in Taiwan: Incidence and Trends (1995-2009).Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcomeEpidemiology and genetics of childhood cancer.Parental infertility, infertility treatment and hepatoblastoma: a report from the Children's Oncology Group.Elevated maternal serum α-fetoprotein level in a fetus with Beckwith-Wiedemann syndrome in the second trimester of pregnancy.Isolated hemihyperplasia in an infant: an overlooked sign for wilms tumor development.The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome.Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression.Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor.Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice.Molar pregnancy and childhood cancer: a population-based linkage study from Denmark.
P2860
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P2860
Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@ast
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@en
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@nl
type
label
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@ast
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@en
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@nl
prefLabel
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@ast
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@en
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@nl
P3181
P1476
Risk of cancer during the firs ...... th-Wiedemann Syndrome Registry
@en
P2093
M A Tucker
M R DeBaun
P304
P3181
P356
10.1016/S0022-3476(98)70008-3
P407
P433
P577
1998-03-01T00:00:00Z