About: Bert Smeets

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

researcher ORCID ID = 0000-0003-1620-908X

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) researcher ORCID ID = 0000-0003-1620-908X (en)
rdfs:label	Bert Smeets (en) Bert Smeets (es) Bert Smeets (nl) Bert Smeets (ast)
skos:prefLabel	Bert Smeets (en) Bert Smeets (es) Bert Smeets (nl) Bert Smeets (ast)
name	Bert Smeets (en) Bert Smeets (es) Bert Smeets (nl) Bert Smeets (ast)
Scopus author ID	wds:Q58639514-92B3DEF3-762E-429C-99F1-CC380D9CA810
Scopus author ID	35432038900
given name	wds:Q58639514-A37D0FC4-07D6-4C74-82E6-D5AE6B130BE7
given name	Bert
instance of	wds:Q58639514-0B75C9FD-2FBB-4562-B12D-7CC091AF8114
instance of	Homo sapiens
skos:altLabel	B. Smeets (nl)
occupation	wds:Q58639514-C15421F4-439B-4D0C-A16A-A506918AE0E4
employer	wds:Q58639514-9BB66FB4-59BD-4F5C-AE59-93F558976F20
place of birth	wds:Q58639514-45044CB8-84EE-48F1-B2FB-28A099B6896B
sex or gender	wds:Q58639514-F1EF19A9-2253-4B95-B5CD-B034C156F55B
date of birth	wds:Q58639514-7145BE1F-EC74-44A2-BF41-6E5A317BB548
family name	wds:Q58639514-92A33894-A175-472E-A87C-B6494EC20E14
occupation	university teacher
employer	Maastricht University
place of birth	Maastricht
sex or gender	male
date of birth	1960-09-30 00:00:00Z (xsd:dateTime)
family name	Smeets
ORCID iD	wds:Q58639514-94833001-4222-48DE-8B8D-81355F6CEC9B
ORCID iD	https://orcid.org/0000-0003-1620-908X
ORCID iD	0000-0003-1620-908X
ResearcherID	wds:Q58639514-11745996-8362-478E-B105-7014DBDBA405
ResearcherID	C-2913-2013
NARCIS researcher ID	wds:Q58639514-1daf9110-50cc-4d05-a6fe-2a251fc643d7
NARCIS researcher ID	PRS1272615
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58639514
is author of	Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2 Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip. Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides
is author of	wds:Q82623030-BD88AA1D-8C23-473E-943A-2AE26004F6CA wds:Q51555279-D3FB5EE5-23C8-478C-9877-AE26DA646AF8 wds:Q69599593-59BB910C-4F6F-4932-87E8-487A7E4D0855 wds:Q24599498-476C37FA-91CD-4916-BAE1-4371A8324B38 wds:Q68505541-4BADBC8C-340B-4207-90D0-9F9777C67382

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