About: Baller Gerold syndrome and Fanconi anaemia

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About: Baller Gerold syndrome and Fanconi anaemia Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 January 1998

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1998 (uk) articolo scientifico (pubblicato il 1998) (it) im Jahr 1998 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1998 (ast) scientific article published on 01 January 1998 (en) artikull shkencor i botuar më 01 janar 1998 (sq)
publication date	wds:Q56380535-3D748D5D-BA46-4B4D-BDB5-6B042433F170
publication date	1998-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56380535-E1950066-DA92-41C7-A3A4-C00CCED44927
language of work or name	English
cites work	wds:Q56380535-04F6B68A-4C6A-4341-A537-A60E0E1A8769 wds:Q56380535-43FD799D-DC76-4225-ADAC-7FFB5F18239F wds:Q56380535-4CA86D73-CED1-43D9-8973-393D90B6A578 wds:Q56380535-5B3AC840-9307-4906-9541-007D9912E0F1 wds:Q56380535-5B590EAC-6C3D-445C-8FEA-3C98F3DEA029 wds:Q56380535-BD9D68DA-686B-451E-A809-B36E0B457788 wds:Q56380535-F6B0AD3E-BECD-4F12-A9B6-AEF081A58908
cites work	Fanconi's anemia--chromosome breakage studies in homozygotes and heterozygotes Phenotypic variability in the Baller-Gerold syndrome: report of a mildly affected patient and review of the literature Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations. Presymptomatic diagnosis of Fanconi's anaemia Somatic segregation and Fanconi anemia Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia). Is there a Baller-Gerold syndrome?
author name string	wds:Q56380535-42E8D343-1746-444E-B926-84BAE65E4F49 wds:Q56380535-65A4568D-F20F-4446-898E-3266F0CBCC14 wds:Q56380535-DCB76712-5E5E-4FAF-A7DD-228CB06BED45
author name string	O W Quarrell C J Harrison E L Maltby
rdfs:label	Baller Gerold syndrome and Fanconi anaemia (en) Baller Gerold syndrome and Fanconi anaemia (nl) Baller Gerold syndrome and Fanconi anaemia (sq)
skos:prefLabel	Baller Gerold syndrome and Fanconi anaemia (en) Baller Gerold syndrome and Fanconi anaemia (nl) Baller Gerold syndrome and Fanconi anaemia (sq)
name	Baller Gerold syndrome and Fanconi anaemia (en) Baller Gerold syndrome and Fanconi anaemia (nl) Baller Gerold syndrome and Fanconi anaemia (sq)
title	wds:Q56380535-8F53BD14-F4EA-443E-B1E1-25C6A3290132
title	Baller Gerold syndrome and Fanconi anaemia (en)
page(s)	wds:Q56380535-CF9EEB93-B140-469D-8C0F-96F91342978C
page(s)	228-229
instance of	wds:Q56380535-8671A49E-8401-4D1F-A1EA-BB466683F3A2
instance of	scholarly article
PubMed ID	wds:Q56380535-C1D9B687-74F6-4DFC-B764-E637B0A7C4CA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9450894
PubMed ID	9450894
published in	wds:Q56380535-57DBC4C8-9896-4FB1-B125-3CF0C401A9DC
published in	American Journal of Medical Genetics Part A
issue	wds:Q56380535-397FC633-649E-458D-B0F8-29D73245F0B1
volume	wds:Q56380535-B7C8A382-BF76-4135-BE58-68DCF0676533
issue	2
volume	75
DOI	wds:Q56380535-429A4B1E-B224-423E-8BAB-9E4F1424FF93
DOI	http://dx.doi.org/10.1002/(SICI)1096-8628(19980113)75:2%3C228::AID-AJMG25%3E3.0.CO;2-Q
DOI	10.1002/(SICI)1096-8628(19980113)75:2<228::AID-AJMG25>3.0.CO;2-Q
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56380535
is cites work of	TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome Fetal exposure to sodium valproate associated with Baller-Gerold syndrome: case report and review of the literature Confounding factors in the diagnosis of Fanconi anaemia
is cites work of	wds:Q77435996-5C12DADC-0A18-4261-A107-13E35EF7316A wds:Q36079343-D4ED97A5-9321-4C5E-A638-068951776C84 wds:Q28296558-F2CA1E66-0358-4FDA-B835-B157BFE08A1D

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