The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2377
- 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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The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome ; volume:14 ; number:1 ; day:31 ; month:1 ; year:2014 ; pages:1-6 ; date:12.2014
BMC neurology ; 14, Heft 1 (31.1.2014), 1-6, 12.2014
- Beteiligte Personen und Organisationen
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McDonell, Laura M.
Warman Chardon, Jodi
Schwartzentruber, Jeremy
Foster, Denise
Beaulieu, Chandree L.
Majewski, Jacek
Bulman, Dennis E.
Boycott, Kym M.
SpringerLink (Online service)
- DOI
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10.1186/1471-2377-14-22
- URN
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urn:nbn:de:1111-2016030334851
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
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Beteiligte
- McDonell, Laura M.
- Warman Chardon, Jodi
- Schwartzentruber, Jeremy
- Foster, Denise
- Beaulieu, Chandree L.
- Majewski, Jacek
- Bulman, Dennis E.
- Boycott, Kym M.
- SpringerLink (Online service)
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