Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing ; volume:11 ; number:1 ; day:22 ; month:3 ; year:2016 ; pages:1-16 ; date:12.2016
Orphanet journal of rare diseases ; 11, Heft 1 (22.3.2016), 1-16, 12.2016
- Urheber
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Calmels, Nadège
- Beteiligte Personen und Organisationen
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Greff, Géraldine
Obringer, Cathy
Kempf, Nadine
GASNIER, Claire
Tarabeux, Julien
Miguet, Marguerite
Baujat, Geneviève
Bessis, Didier
Bretones, Patricia
Cavau, Anne
Digeon, Béatrice
Doco-Fenzy, Martine
Doray, Bérénice
Feillet, François
Gardeazabal, Jesus
Gener, Blanca
Julia, Sophie
Llano-Rivas, Isabel
Mazur, Artur
Michot, Caroline
Renaldo-Robin, Florence
Rossi, Massimiliano
Sabouraud, Pascal
Keren, Boris
Depienne, Christel
Muller, Jean
Mandel, Jean-Louis
Laugel, Vincent
SpringerLink (Online service)
- DOI
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10.1186/s13023-016-0408-0
- URN
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urn:nbn:de:1111-2016032824249
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:58 MESZ
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Beteiligte
- Calmels, Nadège
- Greff, Géraldine
- Obringer, Cathy
- Kempf, Nadine
- GASNIER, Claire
- Tarabeux, Julien
- Miguet, Marguerite
- Baujat, Geneviève
- Bessis, Didier
- Bretones, Patricia
- Cavau, Anne
- Digeon, Béatrice
- Doco-Fenzy, Martine
- Doray, Bérénice
- Feillet, François
- Gardeazabal, Jesus
- Gener, Blanca
- Julia, Sophie
- Llano-Rivas, Isabel
- Mazur, Artur
- Michot, Caroline
- Renaldo-Robin, Florence
- Rossi, Massimiliano
- Sabouraud, Pascal
- Keren, Boris
- Depienne, Christel
- Muller, Jean
- Mandel, Jean-Louis
- Laugel, Vincent
- SpringerLink (Online service)
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