Next generation phenotyping using narrative reports in a rare disease clinical data warehouse
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Next generation phenotyping using narrative reports in a rare disease clinical data warehouse ; volume:13 ; number:1 ; day:31 ; month:5 ; year:2018 ; pages:1-11 ; date:12.2018
Orphanet journal of rare diseases ; 13, Heft 1 (31.5.2018), 1-11, 12.2018
- Urheber
-
Garcelon, Nicolas
- Beteiligte Personen und Organisationen
-
Neuraz, Antoine
Salomon, Rémi
Bahi-Buisson, Nadia
Amiel, Jeanne
Picard, Capucine
Mahlaoui, Nizar
Benoit, Vincent
Burgun, Anita
Rance, Bastien
SpringerLink (Online service)
- DOI
-
10.1186/s13023-018-0830-6
- URN
-
urn:nbn:de:101:1-2018080722044827200360
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:32 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- Garcelon, Nicolas
- Neuraz, Antoine
- Salomon, Rémi
- Bahi-Buisson, Nadia
- Amiel, Jeanne
- Picard, Capucine
- Mahlaoui, Nizar
- Benoit, Vincent
- Burgun, Anita
- Rance, Bastien
- SpringerLink (Online service)
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