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Human Mutation|August 14, 1999
Identification of novel mutations in the PCCB gene in European propionic acidemia patients. Mutation in brief no. 253. OnlineS Muro, P Rodríguez-Pombo, B Pérez, et al.Human Mutation|September 30, 1999
Methylation-sensitive, single-strand conformation analysis (MS-SSCA): A rapid method to screen for and analyze methylationT Bianco, D Hussey, A DobrovicHuman Mutation|September 30, 1999
Molecular characterization of wilson disease in the Sardinian population--evidence of a founder effectG Loudianos, V Dessi, M Lovicu, et al.Human Mutation|September 30, 1999
Threading analysis of the Pitx2 homeodomain: predicted structural effects of mutations causing Rieger syndrome and iridogoniodysgenesisS Banerjee-Basu, A D BaxevanisHuman Mutation|September 30, 1999
Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian ChineseO Ainoon, J Joyce, N Y Boo, et al.Human Mutation|September 30, 1999
Acute intermittent porphyria: characterization of two novel mutations in the porphobilinogen deaminase gene, one amino acid deletion (453-455delAGC) and one splicing aceptor site mutation (IVS8-1G>T)A De Siervi, M Mendez, V E Parera, et al.Human Mutation|September 30, 1999
Somatic mutations of the first 14 exons of APC in hamartomatous polyps of the colonJ C Kim, S A Roh, H C Kim, et al.Human Mutation|September 30, 1999
Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemiaM L Cardoso, E Martins, R Vasconcelos, et al.Human Mutation|May 25, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databasesC R Scriver, P M Nowacki, H LehväslaihoHuman Mutation|May 25, 1999
Molecular genetic study of Pompe disease in Chinese patients in TaiwanT M Ko, W L Hwu, Y W Lin, et al.Pageof 574