High-throughput real-time PCR-based genotyping without DNA purification

[1]  N. Treff,et al.  High-throughput real-time PCR-based genotyping without DNA purification , 2012, BMC Research Notes.

[2]  N. Treff,et al.  Development of TaqMan allelic discrimination based genotyping of large DNA deletions. , 2012, Genomics.

[3]  Victoria Cox,et al.  Comparison of Eight Methods for the Extraction of Bacillus atrophaeus Spore DNA from Eleven Common Interferents and a Common Swab , 2011, PloS one.

[4]  D. Bowden,et al.  Buffy coat specimens remain viable as a DNA source for highly multiplexed genome-wide genetic tests after long term storage , 2011, Journal of Translational Medicine.

[5]  N. Treff,et al.  Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses , 2010, Molecular human reproduction.

[6]  Jürgen Brockmöller,et al.  Amelogenin-based sex identification as a strategy to control the identity of DNA samples in genetic association studies. , 2010, Pharmacogenomics.

[7]  D. Hougaard,et al.  High-throughput genotyping on archived dried blood spot samples. , 2009, Genetic testing and molecular biomarkers.

[8]  F. Wagner,et al.  Cost‐efficient sequence‐specific priming–polymerase chain reaction screening for blood donors with rare phenotypes , 2008, Transfusion.

[9]  A. Mustapha,et al.  Evaluation of four template preparation methods for polymerase chain reaction‐based detection of Salmonella in ground beef and chicken , 2002, Letters in applied microbiology.

[10]  M. Kew,et al.  Comparison of hepatitis B virus DNA extractions from serum by the QIAamp blood kit, GeneReleaser, and the phenol-chloroform method , 1996, Journal of clinical microbiology.

[11]  E. Beutler,et al.  Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[12]  R. Desnick,et al.  Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patients. , 1991, The Journal of clinical investigation.

[13]  C. Férec,et al.  A 3′ splice site consensus sequence mutation in the cystic fibrosis gene , 1990, Human Genetics.

[14]  R. Myerowitz,et al.  The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha-chain of beta-hexosaminidase. , 1988, The Journal of biological chemistry.

[15]  K. Abd-Elsalam,et al.  Rapid and efficient extraction of genomic DNA from differentphytopathogenic fungi using DNAzol reagent , 2004, Biotechnology Letters.

[16]  C. Costigan,et al.  The Major Defect in Ashkenazi Jews with Tay-Sachs Disease Is an Insertion in the Gene for the at-Chain of &Hexosaminidase* , 2001 .

[17]  R. Kaul,et al.  Canavan disease: mutations among Jewish and non-Jewish patients. , 1994, American journal of human genetics.