Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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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
- Classification
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Medizin, Gesundheit
- Creator
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Marco, Elysa Jill
- Contributor
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Aitken, Anne Brandes
Nair, Vishnu Prakas
da Gente, Gilberto
Gerdes, Molly Rae
Bologlu, Leyla
Thomas, Sean
Sherr, Elliott H.
SpringerLink (Online service)
- DOI
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10.1186/s12920-018-0362-x
- URN
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urn:nbn:de:101:1-2018080515471930021230
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:24 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- 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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