WFRF:(Chance S.)
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Additional support that connexin32 is the defect in CMTX1.
- Pericak-Vance, M. (author)
- Bergoffen, J. (author)
- Chance, S. (author)
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- Cochrane, S. (author)
- Exler, M. (author)
- Fain, P. (author)
- Fairweather, N. (author)
- Fischbeck, K. (author)
- Gal, A. (author)
- Haites, N. (author)
- Ioanescu, V. (author)
- Kennerson, M. (author)
- Monaco, A. (author)
- Mostacucuiolo, M (author)
- Nicholson, G. (author)
- Sillen, A (author)
- Haines, J. (author)
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- (creator_code:org_t)
- 1995
- 1995
- English.
- In: Human Heredity. ; 45, s. 121-
- Journal article (peer-reviewed)
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- ref (subject category)
- art (subject category)
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- Bergoffen, J.
- Chance, S.
- Cochrane, S.
- Dahl, N.
- Exler, M.
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- Fain, P.
- Fairweather, N.
- Fischbeck, K.
- Gal, A.
- Haites, N.
- Ioanescu, V.
- Kennerson, M.
- Monaco, A.
- Mostacucuiolo, M
- Nicholson, G.
- Sillen, A
- Haines, J.
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- Human Heredity
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- Uppsala University
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