Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2164
- 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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Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss ; volume:15 ; number:1 ; day:20 ; month:12 ; year:2014 ; pages:1-19 ; date:12.2014
BMC genomics ; 15, Heft 1 (20.12.2014), 1-19, 12.2014
- Creator
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Haraksingh, Rajini R.
- Contributor
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Jahanbani, Fereshteh
Rodriguez-Paris, Juan
Gelernter, Joel
Nadeau, Kari C.
Oghalai, John S.
Schrijver, Iris
Snyder, Michael P.
SpringerLink (Online service)
- DOI
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10.1186/1471-2164-15-1155
- URN
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urn:nbn:de:1111-2016072855039
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:54 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
- Haraksingh, Rajini R.
- Jahanbani, Fereshteh
- Rodriguez-Paris, Juan
- Gelernter, Joel
- Nadeau, Kari C.
- Oghalai, John S.
- Schrijver, Iris
- Snyder, Michael P.
- SpringerLink (Online service)
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