Pages that link to "Q41368408"
Jump to navigation
Jump to search
The following pages link to Slowly but surely towards better scanning for mutations (Q41368408):
Displaying 48 items.
- Chemical cleavage reactions of DNA on solid support: application in mutation detection (Q24801137) (← links)
- Experimental Design in Intraspecific Organelle DNA Sequence Studies III: Statistical Measures of Sampling Success (Q28960392) (← links)
- Polymorphisms in the non-coding region of the human mitochondrial genome in unrelated plateletapheresis donors (Q30664008) (← links)
- A decade of high-resolution liquid chromatography of nucleic acids on styrene-divinylbenzene copolymers (Q30718645) (← links)
- Denaturing high-performance liquid chromatography: A review (Q30991032) (← links)
- Identification of known p53 point mutations by capillary electrophoresis using unique mobility profiles in a blinded study (Q32044630) (← links)
- Random mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods (Q32163857) (← links)
- Assessing the genotoxicity of chronic environmental irradiation by using mitochondrial DNA heteroplasmy in the bank vole (Clethrionomys glareolus) at Chornobyl, Ukraine (Q33445097) (← links)
- Screening practices for mutations in the CFTR gene ABCC7. (Q33825439) (← links)
- Effects of chemical contaminants on genetic diversity in natural populations: implications for biomonitoring and ecotoxicology (Q33933796) (← links)
- Molecular diagnosis of cystic fibrosis (Q34132033) (← links)
- Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms (Q34144292) (← links)
- Mining for SNPs: putting the common variants--common disease hypothesis to the test (Q34189877) (← links)
- Fluorescence-based directed termination PCR: direct mutation characterization without sequencing (Q34231544) (← links)
- Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in Gaucher disease (Q34386597) (← links)
- MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications (Q34390765) (← links)
- Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography (Q34442373) (← links)
- Evidence of a genomic biomarker in normal human epithelial mammary cell line, MCF-10A, that is absent in the human breast cancer cell line, MCF-7 (Q34795262) (← links)
- Development of analytical technology in pharmacogenetic research. (Q35545117) (← links)
- Use of single-strand conformation polymorphism analysis to examine the variability of the rpoS sequence in environmental isolates of Salmonellae (Q39483041) (← links)
- Branch migration inhibition in PCR-amplified DNA: homogeneous mutation detection (Q39546028) (← links)
- Directed termination PCR: a one-step approach to mutation detection (Q39723257) (← links)
- Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations (Q39723322) (← links)
- Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations. (Q40552834) (← links)
- Renewable Standard Reference Material for the Detection of TP53 Mutations (Q40622803) (← links)
- Applications of capillary electrophoresis in DNA mutation analysis of genetic disorders (Q40727315) (← links)
- Mutation scanning methods for the analysis of parasite genes (Q41703023) (← links)
- How Genetic Defects Are Identified (Q41745493) (← links)
- Use of GC clamps in DHPLC mutation scanning (Q42709226) (← links)
- Rapid detection of FGFR3 gene mutation in achondroplasia by DHPLC system-coupling heteroduplex and fluorescence-enhanced primer-extension analysis (Q44954997) (← links)
- Fluorescent chemical cleavage of mismatches for efficient screening of the factor VIII gene (Q45887332) (← links)
- Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene (Q45890208) (← links)
- Screening for mitochondrial DNA heteroplasmy in children at risk for mitochondrial disease (Q46667441) (← links)
- Direct Identification of Each Specific Mutation in Codon 12 and 13 of ci-ki-ras2 by SSCP Analysis (Q47999792) (← links)
- Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotype (Q48494417) (← links)
- Generation of co-dominant PCR-based markers by duplex analysis on high resolution gels (Q51605346) (← links)
- Rapid detection of beta-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC. (Q54757012) (← links)
- Towards Automation for Molecular Diagnosis of Cancer. (Q55283423) (← links)
- A One-Step Prescreening for Point Mutations and Large Rearrangement in BRCA1 and BRCA2 Genes Using Quantitative Polymerase Chain Reaction and High-Resolution Melting Curve Analysis (Q64387069) (← links)
- Micropellicular stationary phases for high-performance liquid chromatography of double-stranded DNA (Q64389087) (← links)
- Isolation and analysis of amplified cDNA fragments during detection of unknown polymorphisms with temperature modulated heteroduplex chromatography (Q73033633) (← links)
- Rapid, accurate genotyping of beta-thalassaemia mutations using a novel multiplex primer extension/denaturing high-performance liquid chromatography assay (Q73626718) (← links)
- A commented dictionary of techniques for genotyping (Q73892756) (← links)
- T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families (Q74457635) (← links)
- Mutation detection by chemical cleavage (Q74618463) (← links)
- Detection of Single Nucleotide Variations (Q74782542) (← links)
- Detection of p53 gene mutations: analysis by single-strand conformation polymorphism and Cleavase fragment length polymorphism (Q77918382) (← links)
- Detection of p53 gene mutations by nonisotopic RNase cleavage assay as a predictor of poor prognosis in colorectal cancers (Q79307475) (← links)