A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning.
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WWOX: a candidate tumor suppressor gene involved in multiple tumor typesFamilial hypercholesterolemia in St-Petersburg: the known and novel mutations found in the low density lipoprotein receptor gene in RussiaRecent developments in high-throughput mutation screening.Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.Sequence analysis of coding and 3' and 5' flanking regions of the epithelial sodium channel alpha, beta, and gamma genes in Dahl S versus R rats.Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography.Haemophilia B: from molecular diagnosis to gene therapy.Important genetic checkpoints for insulin resistance in salt-sensitive (S) Dahl rats.A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL).Inherited hearing loss: molecular genetics and diagnostic testing.Abnormalities of the p53 Tumour Suppressor Gene in Mature B-cell Neoplasms.Genetic variability of immunomodulatory genes in ectromelia virus isolates detected by denaturing high-performance liquid chromatography.Denaturing high-performance liquid chromatography detection of ribosomal mutations conferring macrolide resistance in gram-positive cocciRenewable standard reference material for the detection of TP53 mutations.Validation of denaturing high performance liquid chromatography as a rapid detection method for the identification of human INK4A gene mutations.Analysis of the coding and the 5' flanking regions of the alpha-synuclein gene in patients with Parkinson's disease.Use of TP53 reference materials to validate mutations in clinical tissue specimens by single-strand conformational polymorphism analysis.Pendred syndrome and DFNB4-mutation screening ofSLC26A4by denaturing high-performance liquid chromatography and the identification of eleven novel mutationsAutomated mutation screening using dideoxy fingerprinting and capillary array electrophoresisFurther extension of the H1 haplotype associated with progressive supranuclear palsy
P2860
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P2860
A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning.
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2000 nî lūn-bûn
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A comparison of fluorescent SS ...... throughput mutation scanning.
@en
A comparison of fluorescent SS ...... throughput mutation scanning.
@nl
type
label
A comparison of fluorescent SS ...... throughput mutation scanning.
@en
A comparison of fluorescent SS ...... throughput mutation scanning.
@nl
prefLabel
A comparison of fluorescent SS ...... throughput mutation scanning.
@en
A comparison of fluorescent SS ...... throughput mutation scanning.
@nl
P2093
P2860
P1433
P1476
A comparison of fluorescent SS ...... throughput mutation scanning.
@en
P2093
P2860
P304
P356
10.1002/1098-1004(200006)15:6<556::AID-HUMU7>3.0.CO;2-C
P577
2000-01-01T00:00:00Z