About: Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

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About: Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1980

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1980 (uk) articolo scientifico (pubblicato il 1980) (it) artículu científicu espublizáu en xineru de 1980 (ast) im Januar 1980 veröffentlichter wissenschaftlicher Artikel (de) 1980 թվականի հունվարի 1-ին հրատարակված գիտական հոդված (hy) artikull shkencor i botuar më 01 janar 1980 (sq) scientific article published on 01 January 1980 (en)
publication date	wds:Q71128051-8A43784B-9B03-47BE-B21D-EDBB90B64429
publication date	1980-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71128051-32C37744-04A9-4D12-A7DE-5942AC5A9BB5
language of work or name	English
cites work	wds:Q71128051-167015EC-7F47-4C6B-B92D-41EB452C4816 wds:Q71128051-18E0983A-6E5D-49B4-B956-E7E09AEC95AB wds:Q71128051-1DEA1E3F-5A5B-4251-A4B6-0CA20278B3EB wds:Q71128051-2C3BC8DF-501A-44EA-8B02-CAAC0638229B wds:Q71128051-4EC1E013-2E57-4311-80BF-9E6466F30B53 wds:Q71128051-566EAA4E-5CD5-4DE2-9944-C956843227AC wds:Q71128051-6B35BFE6-7DDD-43EA-AF14-6EC0534B347F wds:Q71128051-81F4D818-4FAD-4738-A692-538BAAC625B8 wds:Q71128051-82807C65-CC07-41C6-A70C-4EA1DEB31F32 wds:Q71128051-87A5218A-E484-4EB4-838A-672A3C3A1A36 wds:Q71128051-8EE7ADA2-64CF-4E5D-9427-1BDEA538FD82 wds:Q71128051-A5BE3976-C682-4C3D-A9BB-5097563D59D1 wds:Q71128051-ACEB4856-F8F4-4195-8208-FA99563148E1 wds:Q71128051-CCCC97EF-BD4A-42E4-B241-51CD84771611 wds:Q71128051-D3A81356-8636-4CD8-AB74-FF1542C71971 wds:Q71128051-DF58C8C4-7BB3-40E4-B90A-DE95E24A44FF
cites work	Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome Adrenocortical neoplasms with hemihypertrophy, brain tumors, and other disorders. Congenital asymmetry (hemihypertrophy) and abdominal disease: radiological features in 9 cases Hepatoblastoma and hepatocarcinoma in infancy and childhood. Report of 47 cases Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases A case of EMG (exomphalos, macroglossia, and gigantism) syndrome with associated renal tumor [Clinical and anatomical findings in hemi-megalencephaly; role of cerebral hyperplasia and of local gigantism associated with phacomatosis] Deficient 17-Hydroxylation in a Corticosterone Producing Adrenal Tumor from an Infant with Hemihypertrophy and Visceromegaly1 Congenital hemihypertrophy and malignancy Medullary sponge kidney associated with congenital hemihypertrophy (asymmetry). A case report and survey of the literature Orthopedic aspects of congenital hypertrophy E.M.G. syndrome Bilateral, diffuse nephroblastomatosis: Report of a case managed with chemotherapy Bilateral nephromegaly in a child with hemihypertrophy
author name string	wds:Q71128051-33C09999-C7AC-4BA4-BE3F-67B7751D333D wds:Q71128051-97FC2D7C-0532-45B8-AD87-17286DA4DADD wds:Q71128051-F59E8A8A-0979-4F43-9DF7-C1916C778A5D
author name string	F Gonzalez-Crussi J W Fowler C Sotelo-Avila
rdfs:label	Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (en) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (nl) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (sq)
skos:prefLabel	Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (en) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (nl) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (sq)
name	Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (en) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (nl) Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (sq)
title	wds:Q71128051-EF16B924-3C7A-469D-9203-0178FB6F2663
title	Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential (en)
page(s)	wds:Q71128051-70CE25D2-1072-46A9-9617-E35F69B61041
page(s)	47-50
instance of	wds:Q71128051-6B469FFC-E34F-4726-837C-E0E0EF23988F
instance of	scholarly article
main subject	wds:Q71128051-A262465B-C53A-4CD7-A342-83F6568D45CF
main subject	Beckwith-Wiedemann syndrome
PubMed ID	wds:Q71128051-D47B2727-54C5-4DC2-AEBA-B435D7676212
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7350313
PubMed ID	7350313
published in	wds:Q71128051-11DDDF1F-E7F4-4DAF-96E2-F06DB9216F13
published in	The Journal of Pediatrics
issue	wds:Q71128051-7BA3B204-704E-41F0-B261-49CE9EE7ECF5
volume	wds:Q71128051-2D1B589A-A7E7-4409-AC6F-19826F3EEF60
issue	1
volume	96
DOI	wds:Q71128051-35BF43EE-A7D1-4EDB-8EB7-7CA398C51154
DOI	http://dx.doi.org/10.1016/S0022-3476(80)80322-2
DOI	10.1016/S0022-3476(80)80322-2
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71128051
is cites work of	Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome Oncogenes and tumor-suppressor genes Genetic and epigenetic losses of heterozygosity in cancer predisposition and progression Association between hepatoblastoma and very low birth weight: a trend or a chance? Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females Somatic overgrowth associated with overexpression of insulin-like growth factor II. Genetic mosaicism in normal tissues of Wilms' tumour patients Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome. Beckwith-Wiedemann syndrome The molecular and genetic characterization of human soft tissue tumors. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells Pathogenesis of adrenocortical incidentalomas and genetic syndromes associated with adrenocortical neoplasms

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