A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2054-345X
- 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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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
- Urheber
-
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
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:56 MESZ
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Beteiligte
- 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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