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Genomics|September 24, 1999
Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1L Feliubadaló, L Bisceglia, M Font, et al.Amino Acids|November 2, 2013
The molecular basis of cystinuria: the role of the rBAT geneM Palacín, C Mora, J Chillarón, et al.European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.American Journal of Human Genetics|March 1, 1997
Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1L Bisceglia, M J Calonge, A Totaro, et al.Human Genetics|October 1, 1996
Molecular analysis of the cystinuria disease gene: identification of four new mutations, one large deletion, and one polymorphismL Bisceglia, M J Calonge, L Dello Strologo, et al.American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 16, 1999
Risk factors for spread of primary adult onset blepharospasm: a multicentre investigation of the Italian movement disorders study groupG Defazio, A Berardelli, G Abbruzzese, et al.Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|October 17, 1998
[The toxicology and prevention of the risks of occupational exposure to aromatic polycyclic hydrocarbons. I. Guide lines for the prevention of the risks of occupational exposure to aromatic polycyclic hydrocarbons. Società Italiana Valori di Riferimento and Cattedra di Medicina del Lavoro, Università di Brescia]L Alessio, P Apostoli, S Porru, et al.Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|February 26, 2004
[Exposure to PAHs, urinary 1-pyrenol and DNA adducts in samples from a population living at different distances from a steel plant]G M Ferri, A Gallo, M Sumerano, et al.Annals of Human Genetics|January 25, 2007
The missing ApoE alleleD Seripa, M G Matera, A Daniele, et al.Pageof 10