Pages that link to "Q24633695"
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The following pages link to Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification (Q24633695):
Displayed 50 items.
- Connector inversion probe technology: a powerful one-primer multiplex DNA amplification system for numerous scientific applications (Q21144430) (← links)
- Real-time PCR in virology (Q24514920) (← links)
- Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis (Q24517912) (← links)
- The elimination of primer-dimer accumulation in PCR (Q24545124) (← links)
- Short-sequence DNA repeats in prokaryotic genomes (Q24548611) (← links)
- Multiplex PCR: optimization and application in diagnostic virology (Q24550705) (← links)
- Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications (Q24605996) (← links)
- Disease-specific induced pluripotent stem cells (Q24641981) (← links)
- Improved molecular diagnostics for ornithine transcarbamylase deficiency (Q24679297) (← links)
- Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector (Q24682774) (← links)
- Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing (Q24794339) (← links)
- Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients (Q24801630) (← links)
- Multiplex PCR: use of heat-stable Thermus thermophilus RecA protein to minimize non-specific PCR products. (Q24811306) (← links)
- MPrime: efficient large scale multiple primer and oligonucleotide design for customized gene microarrays (Q24813613) (← links)
- Multiplex polymerase chain reaction: a practical approach (Q28218083) (← links)
- Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase (Q28291219) (← links)
- Genotoxicity of 3'-azido-3'-deoxythymidine in the human lymphoblastoid cell line, TK6: relationships between DNA incorporation, mutant frequency, and spectrum of deletion mutations in HPRT (Q28374498) (← links)
- Enhanced Reprogramming Efficiency and Kinetics of Induced Pluripotent Stem Cells Derived from Human Duchenne Muscular Dystrophy (Q28550776) (← links)
- Immuno-characterization of the switch of peptide elongation factors eEF1A-1/EF-1alpha and eEF1A-2/S1 in the central nervous system during mouse development (Q28588335) (← links)
- Identification and characterization of new human medium reiteration frequency repeats (Q28776474) (← links)
- Multiplex PCR strategy for rapid identification of structural types and variants of the mec element in methicillin-resistant Staphylococcus aureus (Q30330462) (← links)
- Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion. (Q30444633) (← links)
- Molecular analysis of a spontaneous dystrophin 'knockout' dog. (Q30735735) (← links)
- Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry (Q32133707) (← links)
- Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy (Q33194576) (← links)
- Sensitive detection of SARS coronavirus RNA by a novel asymmetric multiplex nested RT-PCR amplification coupled with oligonucleotide microarray hybridization (Q33223139) (← links)
- PathogenMip assay: a multiplex pathogen detection assay (Q33274668) (← links)
- Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes (Q33511051) (← links)
- Genetic disease detection and DNA amplification using cloned thermostable ligase (Q33513287) (← links)
- The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins (Q33587381) (← links)
- Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy (Q33590398) (← links)
- A TaqI map of the dystrophin gene useful for deletion and carrier status analysis (Q33593612) (← links)
- Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene (Q33593859) (← links)
- Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophy (Q33594356) (← links)
- Identification of a new DMD gene deletion by ectopic transcript analysis (Q33594443) (← links)
- Quantitative Southern blot analysis in the dystrophin gene of Japanese patients with Duchenne or Becker muscular dystrophy: a high frequency of duplications (Q33594787) (← links)
- Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation. (Q33595110) (← links)
- Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups (Q33595755) (← links)
- Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene (Q33596646) (← links)
- A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods (Q33596808) (← links)
- The polymerase chain reaction: current and future clinical applications (Q33596916) (← links)
- Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locus (Q33597918) (← links)
- Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy (Q33597923) (← links)
- Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and Hungary (Q33598261) (← links)
- Measurement of locus copy number by hybridisation with amplifiable probes (Q33612453) (← links)
- Simultaneous detection of genetically modified organisms by multiplex ligation-dependent genome amplification and capillary gel electrophoresis with laser-induced fluorescence (Q33622606) (← links)
- Molecular diagnosis of herpes simplex virus infections in the central nervous system (Q33655137) (← links)
- Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD (Q33678004) (← links)
- Multiplex PCR for typing and subtyping influenza and respiratory syncytial viruses (Q33679059) (← links)
- The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol (Q33679539) (← links)