Author/Creator: Gurgel-Giannetti, J - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Gurgel-Giannetti, J

1. Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Issue 2 (2nd February 2004)

Authors:: Tonini, M M O; Pavanello, R C M; Gurgel-Giannetti, J; Lemmers, R J; van der Maarel, S M; Frants, R R; Zatz, M
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 2(2004)
Page Start:: e17
Record Type:: Journal Article
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2. Low prevalence of PANK2 mutations in Brazilian patients with early onset generalised dystonia and basal ganglia abnormalities on MRI. Issue 9 (15th June 2010)

Authors:: Camargos, S T; Gurgel-Giannetti, J; Lees, A; Hardy, J; Singleton, A; Cardoso, F
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 82:Issue 9(2011)
Page Start:: 1059
Record Type:: Journal Article
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