About: Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma

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About: Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 1986

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1986 (uk) im Oktober 1986 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 1986 (ast) scientific article published on 01 October 1986 (en)
publication date	wds:Q70147637-2DB644C2-BA33-40A3-9749-D4BE505652E1
publication date	1986-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q70147637-C2318911-40AA-4A68-87C5-4E1C15012315 wds:Q70147637-C503C483-204A-4266-A0D0-E053096F923D wds:Q70147637-D9993791-4813-4452-A82C-52B77D7F7F28 wds:Q70147637-F880EA92-11B8-4237-A687-9CDD0EA44BF5
author name string	O A Haas H Gadner A Zoubek E R Grümayer
rdfs:label	Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (en) Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (nl)
skos:prefLabel	Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (en) Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (nl)
name	Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (en) Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (nl)
title	wds:Q70147637-AF651503-60C0-49C7-A4D5-B9766B981F4E
title	Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma (en)
page(s)	wds:Q70147637-6BA638D2-EEEC-4B05-94B2-C3AE1B4F6676
page(s)	95-104
instance of	wds:Q70147637-58BC1726-DA58-4755-AAF5-0AE7B1C1D3B4
instance of	scholarly article
main subject	wds:Q70147637-9CB2A5F5-8D2E-49E1-B048-F5F4C10957FC
main subject	hepatoblastoma
PubMed ID	wds:Q70147637-2BBF6493-6862-4623-9731-5C32349BC783
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3019515
PubMed ID	3019515
published in	wds:Q70147637-C60BDBD0-0E59-440E-B460-65C8258A419C
published in	Cancer Genetics and Cytogenetics
issue	wds:Q70147637-F95AAD83-FD63-4FC7-916C-627B0451C0B5
volume	wds:Q70147637-71208247-3348-4CF1-8E37-62C5E25DB9A0
issue	2
volume	23
DOI	wds:Q70147637-EF29627F-B05D-4E74-88EB-9A07A5B2A6E8
DOI	http://dx.doi.org/10.1016/0165-4608(86)90409-7
DOI	10.1016/0165-4608(86)90409-7
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70147637
is cites work of	Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome Karyotypic analyses of hepatoblastoma. Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease The treatment of hepatoblastoma: Its evolution and the current status as per the SIOPEL trials Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH Localization of a putative liver tumor suppressor locus to a 950-kb region of human 11p11.2-p12 using rat liver tumor microcell hybrid cell lines Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5). Where do we stand with hepatoblastoma? A review Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome. Trisomy 2 and 20 in two hepatoblastomas Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma. Genetic changes in hepatoblastoma Renal and urinary tract abnormalities associated with chromosome aberrations. Significance of extra copies of chromosome 20 and the long arm of chromosome 2 in hepatoblastoma Clinical, molecular- and cytogenetic analysis of a case of severe radio-sensitivity
is cites work of	wds:Q34376509-2E4A47BE-8721-4295-9D82-6186BBD0A640 wds:Q68248441-A57FE7B2-68DE-416C-BB0E-6BFE437B999D wds:Q71708145-9BFC75C4-2554-4BAD-8D0C-456647FBF69B wds:Q40695318-98EAD774-CAA0-49D8-A96B-2C66B9E2B256 wds:Q33596012-D228A904-0F29-4A31-B2C4-3CA5D4A806E4 wds:Q71758606-6F73C1B1-EBB2-453F-91E6-AE7E0EF82A93 wds:Q33754042-82648057-8B7D-4B7E-A440-B714F27C9096 wds:Q39699394-2DD9886B-E4DB-4706-8C4A-AC6F4A8E7E78 wds:Q33593899-29A91300-618D-44C1-BD15-E3FCAB05C668 wds:Q42321079-9E06417D-4385-4102-A1FA-663D7E629D4E wds:Q52220644-3EC58A4B-0DB2-45F3-8E52-768397FC3AC2 wds:Q33679562-3F1D2A92-55D5-4C61-AEAD-A5A231E25931 wds:Q41335659-4836F817-CB1A-4719-B6D0-4FFABDF9B9A3 wds:Q73682741-17E6765C-0335-4A6F-A3E1-B77C22519B6A wds:Q30495385-3FD620DE-ACD7-44C1-A4F2-26BFFD23AE11 wds:Q35248366-EAA1E8A7-C7F8-451F-9DF3-E02441B7BBBC wds:Q35196714-602C7D4E-3C75-4FB8-901E-9BC06DC084E4

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