Author/Creator: Vitelli, F - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Vitelli, F

1. Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR). Issue 5 (1st May 2002)

Authors:: Meloni, I; Vitelli, F; Pucci, L; Lowry, R B; Tonlorenzi, R; Rossi, E; Ventura, M; Rizzoni, G; Kashtan, C E; Pober, B; Renieri, A
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 5(2002)
Page Start:: 359
Record Type:: Journal Article
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2. Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?. Issue 4 (April 1998)

Authors:: Jonsson, J J; Renieri, A; Gallagher, P G; Kashtan, C E; Cherniske, E M; Bruttini, M; Piccini, M; Vitelli, F; Ballabio, A; Pober, B R
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 4(1998)
Page Start:: 273
Record Type:: Journal Article
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