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Cytogenetics and Cell Genetics|July 4, 2001
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogasterA Ratti, F Amati, M Bozzali, et al.Human Mutation|January 1, 1996
Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locusF Capon, C Levato, E Bussaglia, et al.Scandinavian Journal of Haematology|January 1, 1982
Fetal liver transplantation in 2 patients with acute leukaemia after total body irradiationG Lucarelli, T Izzi, A Porcellini, et al.Archives of Disease in Childhood|February 1, 1982
Haemoglobin levels and blood requirement in thalassaemiaV Gabutti, A Piga, P Nicola, et al.Biochemical and Molecular Medicine|June 1, 1997
Expression study of survival motor neuron gene in human fetal tissuesG Novelli, L Calzà, P Amicucci, et al.Nature Genetics|April 1, 1994
Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystineM J Calonge, P Gasparini, J Chillarón, et al.Journal of Medical Genetics|June 30, 2000
Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genesA Botta, G Novelli, A Mari, et al.Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|February 8, 2005
Serum levels of malondialdehyde and 4-hydroxy-2,3-nonenal in patients affected by familial chronic nail candidiasisS Gangemi, A Saija, P L Minciullo, et al.The American Journal of Gastroenterology|December 23, 2008
Polymorphism of the IRGM gene might predispose to fistulizing behavior in Crohn's diseaseA Latiano, O Palmieri, S Cucchiara, et al.American Journal of Human Genetics|March 1, 1994
Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.Pageof 34