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British Journal of Clinical Pharmacology|March 10, 1998
Loratadine-pseudoephedrine in children with allergic rhinitis, a controlled double-blind trialH A Serra, O Alves, L F Rizzo, et al.Human Genetics|September 1, 1990
Cystic fibrosis in Greece: typing with DNA probes and identification of the common molecular defectA Balassopoulou, D Loukopoulos, P Kollia, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|July 4, 2008
High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral densityH Zhang, K Sol-Church, H Rydbeck, et al.Acta Universitatis Carolinae. Medica|January 1, 1990
Preliminary results on cystic fibrosis haplotypes from patients diagnosed in OdessaL De Benedetti, P Ronchetto, M Devoto, et al.Acta Dermato-Venereologica. Supplementum|January 1, 1989
Further characterization of the "incipient lesion of chronic stationary type psoriasis vulgaris in exacerbation". The CD4-positive lymphocytes are the prominent cell population infiltrating the dermisG De Panfilis, G C Manara, C Ferrari, et al.Acta Physiologica, Pharmacologica Et Therapeutica Latinoamericana : Organo De La Asociacion Latinoamericana De Ciencias Fisiologicas Y [De] La Asociacion Latinoamericana De Farmacologia|January 1, 1997
Risk factors for hepatotoxicity induced by antituberculosis drugsF M Devoto, C González, R Iannantuono, et al.Human Molecular Genetics|July 1, 1996
Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharingA Bolino, V Brancolini, F Bono, et al.American Journal of Human Genetics|April 1, 1996
The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28A Auricchio, V Brancolini, G Casari, et al.Genetic Epidemiology|January 17, 2002
Comparison of sib pair-based approaches for identifying quantitative trait loci underlying asthma in the Busselton familiesY Y Shugart, C Specchia, H H Li, et al.Human Molecular Genetics|November 2, 2001
Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36M Devoto, C Specchia, H H Li, et al.Pageof 8