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Artikel
Link zu diesem Datensatz https://d-nb.info/1169742866
Titel Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants / by Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A. Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck, Kate Pope, Els Voorhoeve, Jieun Yoon, Paweł Stankiewicz, Sau Wai Cheung, Damian Pazuchanics, Emily Huber, Vijay Kumar, Rachel L. Kember, Francesca Mari, Aurora Curró, Lucia Castiglia, Ornella Galesi, Emanuela Avola, Teresa Mattina, Marco Fichera, Luana Mandarà, Marie Vincent, Mathilde Nizon, Sandra Mercier, Claire Bénéteau, Sophie Blesson, Dominique Martin-Coignard, Anne-Laure Mosca-Boidron, Jean-Hubert Caberg, Maja Bucan, Susan Zeesman, Małgorzata J. M. Nowaczyk, Mathilde Lefebvre, Laurence Faivre, Patrick Callier, Cindy Skinner, Boris Keren, Charles Perrine, Paolo Prontera, Nathalie Marle, Alessandra Renieri, Alexandre Reymond, R. Frank Kooy, Bertrand Isidor, Charles Schwartz, Corrado Romano, Erik Sistermans, David J. Amor, Joris Andrieux, Santhosh Girirajan
Person(en) Pizzo, Lucilla (Verfasser)
Jensen, Matthew (Sonstige)
Polyak, Andrew (Sonstige)
Rosenfeld, Jill A. (Sonstige)
Mannik, Katrin (Sonstige)
Krishnan, Arjun (Sonstige)
McCready, Elizabeth (Sonstige)
Pichon, Olivier (Sonstige)
Caignec, Cedric Le (Sonstige)
Dijck, Anke Van (Sonstige)
Pope, Kate (Sonstige)
Voorhoeve, Els (Sonstige)
Yoon, Jieun (Sonstige)
Stankiewicz, Paweł (Sonstige)
Cheung, Sau Wai (Sonstige)
Pazuchanics, Damian (Sonstige)
Huber, Emily (Sonstige)
Kumar, Vijay (Sonstige)
Kember, Rachel L. (Sonstige)
Mari, Francesca (Sonstige)
Curró, Aurora (Sonstige)
Castiglia, Lucia (Sonstige)
Galesi, Ornella (Sonstige)
Avola, Emanuela (Sonstige)
Mattina, Teresa (Sonstige)
Fichera, Marco (Sonstige)
Mandarà, Luana (Sonstige)
Vincent, Marie (Sonstige)
Nizon, Mathilde (Sonstige)
Mercier, Sandra (Sonstige)
Bénéteau, Claire (Sonstige)
Blesson, Sophie (Sonstige)
Martin-Coignard, Dominique (Sonstige)
Mosca-Boidron, Anne-Laure (Sonstige)
Caberg, Jean-Hubert (Sonstige)
Bucan, Maja (Sonstige)
Zeesman, Susan (Sonstige)
Nowaczyk, Małgorzata J. M. (Sonstige)
Lefebvre, Mathilde (Sonstige)
Faivre, Laurence (Sonstige)
Callier, Patrick (Sonstige)
Skinner, Cindy (Sonstige)
Keren, Boris (Sonstige)
Perrine, Charles (Sonstige)
Prontera, Paolo (Sonstige)
Marle, Nathalie (Sonstige)
Renieri, Alessandra (Sonstige)
Reymond, Alexandre (Sonstige)
Kooy, R. Frank (Sonstige)
Isidor, Bertrand (Sonstige)
Schwartz, Charles (Sonstige)
Romano, Corrado (Sonstige)
Sistermans, Erik (Sonstige)
Amor, David J. (Sonstige)
Andrieux, Joris (Sonstige)
Girirajan, Santhosh (Sonstige)
Organisation(en) SpringerLink (Online service) (Sonstige)
Umfang/Format Online-Ressource : online resource.
Persistent Identifier URN: urn:nbn:de:101:1-2018102402155511340863
DOI: 10.1038/s41436-018-0266-3
URL http://dx.doi.org/10.1038/s41436-018-0266-3
Zeitliche Einordnung Erscheinungsdatum: 2018
DDC-Notation 616.042 (maschinell ermittelte DDC-Kurznotation)
Sprache(n) Englisch (eng)
Beziehungen Enthalten in: Genetics in medicine (7.9.2018: 1-10)
Sachgruppe(n) 610 Medizin, Gesundheit

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