Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- 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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Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction ; volume:11 ; number:1 ; day:25 ; month:5 ; year:2018 ; pages:1-11 ; date:12.2018
BMC medical genomics ; 11, Heft 1 (25.5.2018), 1-11, 12.2018
- Klassifikation
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Medizin, Gesundheit
- Urheber
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Marco, Elysa Jill
- Beteiligte Personen und Organisationen
-
Aitken, Anne Brandes
Nair, Vishnu Prakas
da Gente, Gilberto
Gerdes, Molly Rae
Bologlu, Leyla
Thomas, Sean
Sherr, Elliott H.
SpringerLink (Online service)
- DOI
-
10.1186/s12920-018-0362-x
- URN
-
urn:nbn:de:101:1-2018080515471930021230
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:24 MESZ
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Beteiligte
- Marco, Elysa Jill
- Aitken, Anne Brandes
- Nair, Vishnu Prakas
- da Gente, Gilberto
- Gerdes, Molly Rae
- Bologlu, Leyla
- Thomas, Sean
- Sherr, Elliott H.
- SpringerLink (Online service)
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