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You searched for: Author/Creator Chiavacci, Rosetta M

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1. Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease. Issue 8 (11th July 2007)

2. Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome. Issue 2 (20th November 2014)