About: HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES 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 March 1964

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1964 (uk) im März 1964 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1964 (ast) scientific article published on 01 March 1964 (en) 1964 թվականի մարտի 1-ին հրատարակված գիտական հոդված (hy)
publication date	wds:Q76753587-4204DAA1-E252-406D-98A6-E41B634B8622
publication date	1964-03-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q76753587-0A660477-2875-4C2C-890B-E66720A35872 wds:Q76753587-1C56B14D-6D66-4B66-AD1A-3B97C1722B00 wds:Q76753587-8F3F8B84-E800-4939-862D-89B7A1FD427F
author name string	G HABIB P F LABAND G S HUMPHREYS
rdfs:label	HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (en) HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (nl)
skos:prefLabel	HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (en) HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (nl)
name	HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (en) HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (nl)
title	wds:Q76753587-05881A1C-9D03-4992-8F7F-9398A66371B2
title	HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES (en)
page(s)	wds:Q76753587-E475BABF-2D68-40D7-86E4-05333B4BC406
page(s)	339-351
instance of	wds:Q76753587-763CACB0-ED11-4F49-B18B-CEA23CC10892
instance of	scholarly article
PubMed ID	wds:Q76753587-CE93A18E-953A-426E-9C12-D50029EC50B0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14130237
PubMed ID	14130237
published in	wds:Q76753587-0C8BEC81-72D2-4C5D-9BE2-B9B3F6926966
published in	Oral surgery, oral medicine, and oral pathology
volume	wds:Q76753587-25818323-1297-4695-8C71-90C9E4E0E867
volume	17
DOI	wds:Q76753587-A8375CE8-4D6F-4D5D-8245-C9E96FA64D7F
DOI	http://dx.doi.org/10.1016/0030-4220(64)90506-7
DOI	10.1016/0030-4220(64)90506-7
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q76753587
is cites work of	The Coffin-Siris syndrome. A report of four cases and review of the literature Gingival fibromatosis combined with cherubism Inherited hypertrichoses. Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21. A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities Zimmermann-Laband syndrome with bilateral developmental cataract - a new association? Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome. Hereditary gingival fibromatosis Zimmermann-Laband syndrome in an adult. Long-term follow-up of a patient with vascular and cardiac complications Laband syndrome: a case report Eag1 K+ Channel: Endogenous Regulation and Functions in Nervous System. Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome Gingival fibromatosis: clinical, molecular and therapeutic issues Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15 ‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes Hereditary gingival fibromatosis: Characteristics and treatment approach. Gene expression profiling and bioinformatics analysis of hereditary gingival fibromatosis. Congenital idiopathic gingival fibromatosis in the deciduous dentition
is cites work of	wds:Q58443483-0F32080F-8619-4B7B-85D5-777159E3543B wds:Q70922580-8AD3323A-E016-4C36-AA55-EF01BEAE7B25 wds:Q34385103-6AC3A102-9632-4260-80CE-9F164CD3FDD7 wds:Q37711718-B0D396E2-45E5-4C38-90F6-1E8EBEABCD2B wds:Q86385415-AB6B73C9-AD0C-4C0F-AAC5-C8D464AFAF93 wds:Q28067236-4024B3A3-4945-4BC0-92B4-03DC02CA9859 wds:Q49890193-81B1AAFA-698A-49EB-9DF9-2FA98D5EA012 wds:Q40310129-4C782279-19B5-4676-9B98-1ABCC7E17B2E wds:Q56568065-6FEA4D6A-1A85-428C-8516-0421470422B5 wds:Q68618698-F7E9E661-29B5-4669-866C-E71BA641486D wds:Q34191378-B1E00817-E3D1-41E1-9645-64E5CDA13D72 wds:Q67878837-8E34A981-8DDB-4652-A798-1BE373543D3F wds:Q70909603-49BAC70D-6341-43D7-A83D-551B529F1EF1 wds:Q34703656-986ECA19-20ED-4C9C-A010-6ADD78B33846 wds:Q35620693-C1DD9AE7-AAAC-439C-8D37-76A270212AEA wds:Q41010224-5834F607-3188-46C4-A4C3-A86828C95F44 wds:Q41956598-D03F18C6-7C41-4642-A7C6-B2F5463D1234 wds:Q79318008-521425C8-C1FD-45B6-85AC-62731156D43A wds:Q92471065-AB1E8378-BA75-42F6-A91A-073EF666F236

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 196 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software