Pages that link to "Q35222182"
Jump to navigation
Jump to search
The following pages link to Detection of single DNA base differences by competitive oligonucleotide priming (Q35222182):
Displaying 50 items.
- PAX6 gene variations associated with aniridia in south India (Q21261462) (← links)
- Isolation of a cDNA clone of the 14-kDa subunit of the signal recognition particle by cross-hybridization of differently primed polymerase chain reactions (Q24313424) (← links)
- Selective amplification of an mRNA and related pseudogene for a human ADP-ribosylation factor, a guanine nucleotide-dependent protein activator of cholera toxin (Q24558739) (← links)
- Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease (Q24561673) (← links)
- PCR-based methods for the enrichment of minority alleles and mutations (Q24657701) (← links)
- beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosis (Q28242331) (← links)
- Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy (Q33597770) (← links)
- Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. (Q33598200) (← links)
- Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction (Q33635397) (← links)
- A PCR-based method for detection and quantification of small RNAs (Q34000708) (← links)
- Single tube genotyping of sickle cell anaemia using PCR-based SNP analysis (Q34001497) (← links)
- Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources (Q34301388) (← links)
- Overlapping PCR for bidirectional PCR amplification of specific alleles: a rapid one-tube method for simultaneously differentiating homozygotes and heterozygotes (Q34428443) (← links)
- Single base pair mutation analysis by PNA directed PCR clamping (Q35018602) (← links)
- Techniques patents for SNP genotyping (Q35040891) (← links)
- Genetic studies to characterize the origin of the mutation in placental aromatase deficiency (Q35195768) (← links)
- Impaired hepatic apolipoprotein B and E translation in streptozotocin diabetic rats (Q35601708) (← links)
- Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing(CAS) (Q35800977) (← links)
- Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR (Q35927120) (← links)
- Variation in CCL3L1 copy number in rhesus macaques (Macaca mulatta) (Q36000785) (← links)
- Molecular genetic approaches to the analysis and diagnosis of human inherited disease: an overview (Q36067195) (← links)
- Rapid screening of genetic polymorphisms using buccal cell DNA with detection by matrix‐assisted laser desorption/ionization mass spectrometry (Q36692160) (← links)
- Utility of PCR for DNA analysis from dried blood spots on filter paper blotters (Q37144841) (← links)
- Application of the polymerase chain reaction to the diagnosis of human genetic disease (Q37935121) (← links)
- Mutational analysis of human NRAS genes in malignant melanoma: rapid methods for oligonucleotide hybridization and manual and automated direct sequencing of products generated by the polymerase chain reaction (Q38025777) (← links)
- Effect of single mismatches at 3'-end of primers on polymerase chain reaction. (Q38476946) (← links)
- Dystrophin. The gene and its product (Q38645497) (← links)
- Detection of single base changes in nucleic acids (Q38747523) (← links)
- Antenatal diagnosis of pediatric surgical anomalies. Counseling the family. (Q40384549) (← links)
- Detection of point mutations with a modified ligase chain reaction (Gap-LCR). (Q40393131) (← links)
- High-density multiplex detection of nucleic acid sequences: oligonucleotide ligation assay and sequence-coded separation (Q40401832) (← links)
- Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection (Q40408816) (← links)
- Influence of nearest neighbor sequence on the stability of base pair mismatches in long DNA; determination by temperature-gradient gel electrophoresis (Q40412931) (← links)
- Current methods of mutation detection (Q40484307) (← links)
- Chasing behaviour genes into the next millennium (Q40782589) (← links)
- DNA Enrichment by Allele-Specific Hybridization (DEASH): A Novel Method for Haplotyping and for Detecting Low-Frequency Base Substitutional Variants and Recombinant DNA Molecules (Q40830086) (← links)
- Biochemical basis of DNA replication fidelity (Q40903454) (← links)
- Advances in the prenatal and molecular diagnosis of the hemoglobinopathies and thalassemias (Q40932692) (← links)
- Strategies and applications of DNA level diagnosis in genetic diseases: past experiences and future directions. (Q40953874) (← links)
- Analysis of MAOA mutations in humans. (Q40960442) (← links)
- Amplification methods in the molecular diagnosis of genetic diseases. (Q41136691) (← links)
- Genotypic selection methods for the direct analysis of point mutations (Q41645720) (← links)
- A simple method for screening bacterial colonies for mutagenized sites in plasmid DNA. (Q43782952) (← links)
- A new approach for point mutation detection based on a ligase chain reaction (Q43803475) (← links)
- Detection of beta-thalassemia mutations by ASO hybridization of PCR amplified DNA with digoxigenin ddUTP labeled oligonucleotides (Q43805633) (← links)
- Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common β-thalassaemia mutations in Mediterraneans (Q45300442) (← links)
- Strategies for the detection of potential beet necrotic yellow vein virus genome recombinations which might arise as a result of growing A type coat protein gene-expressing sugarbeets in soil containing B type virus (Q45654991) (← links)
- Multiplex genotype determination at a DNA sequence polymorphism cluster in the human immunoglobulin heavy-chain region (Q45936282) (← links)
- Phytochrome of the green alga Mougeotia: cDNA sequence, autoregulation and phylogenetic position (Q48058122) (← links)
- New, Improved Version of the mCOP-PCR Screening System for Detection of Spinal Muscular Atrophy Gene (SMN1) Deletion (Q50055739) (← links)