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American Journal of Medical Genetics|January 9, 2001
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasiaP Iughetti, L G Alonso, W Wilcox, et al.Archives of Insect Biochemistry and Physiology|January 1, 1996
Musca domestica hemolymph ferritinM de L Capurro, P Iughetti, P E Ribolla, et al.Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.Arquivos De Neuro-Psiquiatria|June 16, 2001
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17R Nitrini, L S Teixeira da Silva, S Rosemberg, et al.Annals of Neurology|August 1, 1997
Familial spongiform encephalopathy associated with a novel prion protein gene mutationR Nitrini, S Rosemberg, M R Passos-Bueno, et al.Journal of Medical Genetics|February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesM R Passos-Bueno, E S Moreira, S K Marie, et al.Cancer Research|October 19, 2001
A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinomaP Iughetti, O Suzuki, P H Godoi, et al.Pageof 1