About: Roelof-Jan Oostra

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) investigador (es) araştırmacı (tr) chercheur (fr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt)
exact match	wds:Q37378930-AFB47660-0C1E-4F87-A1E5-7818B604DAF4
exact match	https://scigraph.springernature.com/person.01053161761.91
rdfs:label	Roelof-Jan Oostra (en) Roelof-Jan Oostra (es) Roelof-Jan Oostra (nl) Roelof-Jan Oostra (sl) Roelof-Jan Oostra (ast)
skos:prefLabel	Roelof-Jan Oostra (en) Roelof-Jan Oostra (es) Roelof-Jan Oostra (nl) Roelof-Jan Oostra (sl) Roelof-Jan Oostra (ast)
name	Roelof-Jan Oostra (en) Roelof-Jan Oostra (es) Roelof-Jan Oostra (nl) Roelof-Jan Oostra (sl) Roelof-Jan Oostra (ast)
Scopus author ID	wds:Q37378930-F4B8B26E-7047-4EC1-BA64-681C4AB8DB7A
Scopus author ID	7004875046
instance of	wds:Q37378930-693CE868-C486-40C0-86AC-8B5BB6BB5514
instance of	Homo sapiens
Nationale Thesaurus voor Auteursnamen ID	wds:Q37378930-da3acac8-8ce2-449b-b4e3-5cb045f41665
occupation	wds:Q37378930-19E21F8E-983F-4A11-9139-DE913BB1B210
employer	wds:Q37378930-B3F7E22D-06CF-46AB-AE31-ABE0EFBF2C50
sex or gender	wds:Q37378930-4A9D668C-88CD-4145-8453-05D766BAC833
ISNI	wds:Q37378930-8A5AD8D5-15E4-439A-9563-144224FAAF14
VIAF ID	wds:Q37378930-152B79DB-4BAC-43E1-AAAD-18188287C0A8
Library of Congress authority ID	wds:Q37378930-3AEF006A-FDB7-422A-9081-274F30AB3E3B
WorldCat Identities ID (superseded)	wds:Q37378930-F1C05DFD-D1B1-4265-9813-FC7C9EEE2559
National Library of Israel J9U ID	wds:Q37378930-464267F8-AA07-44C4-87BD-32FBF83B902A
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p151617643
VIAF ID	http://viaf.org/viaf/51133918
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2007013676
Nationale Thesaurus voor Auteursnamen ID	151617643
occupation	researcher
employer	Academic Medical Center
sex or gender	male
ISNI	0000000036100928
VIAF ID	51133918
Library of Congress authority ID	n2007013676
WorldCat Identities ID (superseded)	lccn-n2007013676
National Library of Israel J9U ID	987007362463505171
ORCID iD	wds:Q37378930-159A41B7-4011-4E0D-8A68-D9FC7EF39023
Dimensions author ID	wds:Q37378930-99B182D6-70F6-4E37-B431-9CEE819D9F97
ORCID iD	https://orcid.org/0000-0002-2452-8307
ORCID iD	0000-0002-2452-8307
Dimensions author ID	01053161761.91
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37378930
is author of	An interactive three-dimensional digital atlas and quantitative database of human development A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy. Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome. Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells Smith-Lemli-Opitz syndrome diagnosed in a 130-year-old anatomical specimen. Brachmann-de Lange syndrome "avant la lettre". Severe acrofacial dysostosis with orofacial clefting and tetraphocomelia diagnosed in the plaster cast of a 100-year-old anatomical specimen The anatomy in relation to injury of the lateral collateral ligaments of the ankle: a current concepts review. When the right (Drug) should be left: Prenatal drug exposure and heterotaxy syndrome In patients with pseudoxanthoma elasticum a thicker and more elastic carotid artery is associated with elastin fragmentation and proteoglycans accumulation Pectus excavatum and carinatum Towards a 3-dimensional atlas of the developing human embryo: the Amsterdam experience The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal A review of the embryological development and associated developmental abnormalities of the sternum in the light of a rare palaeopathological case of sternal clefting Reply to Hofmann et al. Postmortem imaging exposed: an aid in MR imaging of musculoskeletal structures Malformations of the axial skeleton in the museum Vrolik: II: craniosynostoses and suture-related conditions Development of the hearts of lizards and snakes and perspectives to cardiac evolution The hypertrabeculated (noncompacted) left ventricle is different from the ventricle of embryos and ectothermic vertebrates. The development of the human notochord [Leber's optic nerve atrophy; a mitochondrial hereditary disease] Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy

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