WFRF:(Gualandi F)
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- Bigoni, S (author)
The novel versican p.H2665L homozygous variation is associated with absence of cementum, early teeth loss and recessive Wagner vitreoretinopathy
- Article/chapterEnglish2019
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- 2019
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:142084115
- http://kipublications.ki.se/Default.aspx?queryparsed=id:142084115URI
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- Language:English
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- Neri, M (author)
- Scotton, C (author)
- Farina, R (author)
- Sabatelli, P (author)
- Jiang, C (author)
- Zhang, J (author)
- Falzarano, M (author)
- Rossi, R (author)
- Ognibene, D (author)
- Selvatici, R (author)
- Gualandi, F (author)
- Bosshardt, D (author)
- Perri, P (author)
- Campa, C (author)
- Brancati, F (author)
- Salvatore, M (author)
- De Stefano, M (author)
- Taruscio, D (author)
- Trombelli, L (author)
- Fang, M (author)
- Ferlini, A (author)
Related titles
- In:EUROPEAN JOURNAL OF HUMAN GENETICS27, s. 1894-18951018-4813
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- Zhang, J
- Falzarano, M
- Rossi, R
- Ognibene, D
- Selvatici, R
- Gualandi, F
- Bosshardt, D
- Perri, P
- Campa, C
- Brancati, F
- Salvatore, M
- De Stefano, M
- Taruscio, D
- Trombelli, L
- Fang, M
- Ferlini, A
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