A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2054-345X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features ; volume:6 ; number:1 ; day:2 ; month:4 ; year:2019 ; pages:1-4 ; date:12.2019
Human genome variation ; 6, Heft 1 (2.4.2019), 1-4, 12.2019
- Creator
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Murata, Yuka
Kurosaka, Hiroshi
Ohata, Yasuhisa
Aikawa, Tomonao
Takahata, Sosuke
Fujii, Katsunori
Miyashita, Toshiyuki
Morita, Chisato
Inubushi, Toshihiro
Kubota, Takuo
Sakai, Norio
Ozono, Keiichi
Kogo, Mikihiko
Yamashiro, Takashi
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41439-019-0047-9
- URN
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urn:nbn:de:101:1-2019042222130368347045
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:56 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
- Murata, Yuka
- Kurosaka, Hiroshi
- Ohata, Yasuhisa
- Aikawa, Tomonao
- Takahata, Sosuke
- Fujii, Katsunori
- Miyashita, Toshiyuki
- Morita, Chisato
- Inubushi, Toshihiro
- Kubota, Takuo
- Sakai, Norio
- Ozono, Keiichi
- Kogo, Mikihiko
- Yamashiro, Takashi
- SpringerLink (Online service)
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