WFRF:(Jagannathan V)
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Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
- Hytonen, MK (author)
- Arumilli, M (author)
- Lappalainen, AK (author)
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- Owczarek-Lipska, M (author)
- Jagannathan, V (author)
- Hundi, S (author)
- Salmela, E (author)
- Venta, P (author)
- Sarkiala, E (author)
- Jokinen, T (author)
- Gorgas, D (author)
- Nieminen, P (author)
- Drogemuller, C (author)
- Lohi, H (author)
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- (creator_code:org_t)
- 2016-05-17
- 2016
- English.
- In: PLoS genetics. - : Public Library of Science (PLoS). - 1553-7404. ; 12:5, s. e1006037-
- Journal article (peer-reviewed)
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- Hytonen, MK
- Arumilli, M
- Lappalainen, AK
- Owczarek-Lipska, ...
- Jagannathan, V
- Hundi, S
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- Salmela, E
- Venta, P
- Sarkiala, E
- Jokinen, T
- Gorgas, D
- Kere, J
- Nieminen, P
- Drogemuller, C
- Lohi, H
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- PLoS genetics
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- Karolinska Institutet
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