Showing results (3151-3160 of 5,826) with videos related to
Sort By:
Pageof 583
Human Mutation|November 3, 2000
Mutation analysis of the hamartin gene using denaturing high performance liquid chromatographyP Bénit, A Kara-Mostefa, M Berthelon, et al.Human Mutation|November 3, 2000
Six novel MEN1 gene mutations in sporadic parathyroid tumorsF Cetani, E Pardi, A Giovannetti, et al.Human Mutation|October 26, 1999
Comparison of heteroduplex analysis, direct sequencing, and enzyme mismatch cleavage for detecting mutations in a large gene, FBN1B Yuan, J P Thomas, Y von Kodolitsch, et al.Human Mutation|September 12, 2000
Activating and inactivating mutations in the human GNAS1 geneM A Aldred, R C TrembathHuman Mutation|September 12, 2000
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexinsR Rabionet, P Gasparini, X EstivillHuman Mutation|September 12, 2000
8th International HUGO-Mutation Database Initiative Meeting, April 9, 2000, Vancouver, CanadaA D AuerbachHuman Mutation|September 12, 2000
A cluster of lysinuric protein intolerance (LPI) patients in a northern part of Iwate, Japan due to a founder effect. The Mass Screening GroupA Koizumi, Y Shoji, J Nozaki, et al.Human Mutation|September 12, 2000
Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY)S Ellard, M P Bulman, T M Frayling, et al.Human Mutation|February 17, 2001
Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuriaA Acosta, W Silva, T Carvalho, et al.Human Mutation|February 17, 2001
Data mining: Efficiency of using sequence databases for polymorphism discoveryD Cox, C Boillot, F CanzianPageof 583