Pages that link to "Q40550432"

The following pages link to Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene (Q40550432):

Displaying 50 items.

• The elimination of primer-dimer accumulation in PCR (Q24545124) (← links)
• AFLP: a new technique for DNA fingerprinting (Q24620887) (← links)
• Fluorescent duplex allele-specific PCR and amplicon melting for rapid homogeneous mtDNA haplogroup H screening and sensitive mixture detection (Q33519569) (← links)
• Prevalence of cystic fibrosis mutations in the Grampian region of Scotland (Q33595220) (← links)
• Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D (Q33677715) (← links)
• Development of a rapid DNA screening procedure for the Factor V Leiden mutation (Q33842391) (← links)
• Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype (Q34001834) (← links)
• Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype (Q34124030) (← links)
• A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis (Q34141568) (← links)
• Reversal of cystic fibrosis phenotype in a cultured Delta508 cystic fibrosis transmembrane conductance regulator cell line by oligonucleotide insertion. (Q34332264) (← links)
• Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families. (Q34350444) (← links)
• Single gene disorders affecting the gastrointestinal tract (Q34377128) (← links)
• CFTR Gene Mutations and Asthma in Indian Children: A Case-Control Study (Q35028057) (← links)
• The polymerase chain reaction: a tool for molecular medicine (Q35186301) (← links)
• Cystic fibrosis carrier testing in early pregnancy by general practitioners (Q35188384) (← links)
• Uptake of cystic fibrosis testing in primary care: supply push or demand pull? (Q35188406) (← links)
• Estimation of the incidence of a rare genetic disease through a two-tier mutation survey (Q35194753) (← links)
• The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women (Q35238946) (← links)
• The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques (Q35573352) (← links)
• The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system (Q36292380) (← links)
• Active cascade testing for carriers of cystic fibrosis gene (Q36885761) (← links)
• Antenatal screening for cystic fibrosis: a trial of the couple model (Q36885781) (← links)
• Allele-Specific Quantitative PCR for Accurate, Rapid, and Cost-Effective Genotyping. (Q37061245) (← links)
• Diagnosis of neonatal group B Streptococcus sepsis by nested-PCR of residual urine samples. (Q37159091) (← links)
• Allele-Specific PCR Method Based on pncA and oxyR Sequences for Distinguishing Mycobacterium bovis from Mycobacterium tuberculosis : Intraspecific M. bovis pncA Sequence Polymorphism (Q38554144) (← links)
• Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis (Q39585577) (← links)
• Rapid detection of rpoB gene mutations in rifampin-resistant Mycobacterium tuberculosis isolates in shanghai by using the amplification refractory mutation system (Q39735446) (← links)
• Human histocompatibility leukocyte antigen-binding supermotifs predict broadly cross-reactive cytotoxic T lymphocyte responses in patients with acute hepatitis (Q39787946) (← links)
• Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection (Q40408816) (← links)
• Chronic pancreatitis: A new pathophysiology. (Q40783589) (← links)
• Expression and regulation of superoxide dismutase activity in human skin fibroblasts from donors of different ages (Q41266938) (← links)
• Evaluation of laboratory methods for cystic fibrosis carrier screening: reliability, sensitivity, specificity, and costs (Q41814756) (← links)
• A mutation-specific PCR system to detect sequence variation in the dihydropteroate synthetase gene of Plasmodium falciparum (Q41933285) (← links)
• Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor gene (Q41952976) (← links)
• Use of chimeric DNA-RNA primers in quantitative PCR for detection of Ehrlichia canis and Babesia canis (Q42570372) (← links)
• Failure to refer for testing for cystic fibrosis. Doctors must ensure that those with a family history are advised appropriately (Q42770608) (← links)
• Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran (Q42964333) (← links)
• Cystic fibrosis genotypes and views on screening are both heterogeneous and population related (Q43146329) (← links)
• Detection of mutations associated with multidrug-resistantMycobacterium tuberculosisclinical isolates (Q44401534) (← links)
• Expanded newborn screening in Greece: 30 months of experience. (Q51755510) (← links)
• A novel compound-primed multiplex ARMS-PCR (CPMAP) for simultaneous detection of common PAH gene mutations. (Q52608177) (← links)
• Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients. (Q54645915) (← links)
• Amplification refractory mutation system PCR assays for the detection of variola and Orthopoxvirus. (Q54725956) (← links)
• Frequency of CFTR, SPINK1, and cathepsin B gene mutation in North Indian population: connections between genetics and clinical data. (Q55311728) (← links)
• Mucopolysaccharidosis type I in 21 Czech and Slovak patients: mutation analysis suggests a functional importance of C-terminus of the IDUA protein. (Q55412955) (← links)
• Cystic Fibrosis Newborn Screening in Portugal: PAP Value in Populations with Stringent Rules for Genetic Studies (Q57761924) (← links)
• The genetic basis of disease (Q59795578) (← links)
• Allele-specific PCR analysis for detection of the gld Fas-ligand point mutation (Q74314647) (← links)
• A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population (Q89477973) (← links)
• Nuclease-Assisted Minor Allele Enrichment Using Overlapping Probes-Assisted Amplification-Refractory Mutation System: An Approach for the Improvement of Amplification-Refractory Mutation System-Polymerase Chain Reaction Specificity in Liquid Biopsie (Q90187687) (← links)