Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2090-2441
- 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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Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects ; volume:21 ; number:1 ; day:30 ; month:10 ; year:2020 ; pages:1-10 ; date:12.2020
The Egyptian journal of medical human genetics ; 21, Heft 1 (30.10.2020), 1-10, 12.2020
- Creator
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Gholipoorfeshkecheh, Rahim
Agarwala, Swati
G, Kavya
Krishnappa, Santhosh
Savitha, Mysore R.
Ramachandra, Nallur B.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s43042-020-00101-4
- URN
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urn:nbn:de:101:1-2020121020283665093624
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Gholipoorfeshkecheh, Rahim
- Agarwala, Swati
- G, Kavya
- Krishnappa, Santhosh
- Savitha, Mysore R.
- Ramachandra, Nallur B.
- SpringerLink (Online service)
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