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Genetic Fingerprinting

Known as: Fingerprintings, Genetic, Genetic Fingerprintings, Fingerprinting, Genetic 
National Institutes of Health

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DNA Fingerprinting

Papers overview

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2018
2018
Poster : Using Packet Timing in Website Fingerprinting
Website Fingerprinting (WF) enables an eavesdropper to discover what sites the user is visiting despite the use of a VPN or even… 
2001
2001
Mutation screening of the neurogenin-3 gene in autosomal dominant diabetes.
We investigated whether genetic variability in neurogenin-3, a basic helix-loop-helix transcription factor that is expressed in… 
1999
1999
Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF).
1999
1999
Screening for Mutations in the Dideoxy Fingerprinting (ddF) GH-1 Gene by
Department of Pediatrics, The Jikei University School of Medicine, Tokyo 105-8461, *Department of Pediatrics , Kami-iida Daiichi… 
1998
1998
Limited allelic polymorphism in the human interleukin-3 gene.
Interleukin-3 (IL-3) is a cytokine expressed primarily in activated T cells mast cells and natural killer (NK) cells. Interleukin… 
1998
1998
Dideoxy fingerprinting for rapid screening of rpoB gene mutations in clinical isolates of Mycobacterium tuberculosis.
Rifampin is a key component of therapeutic regimens for tuberculosis control, and a marker for multidrug resistance of… 
1998
1998
Lack of association between mutations in the folate receptor-alpha gene and spina bifida.
Defects of neural tube closure are among the most common of all human malformations. Epidemiological and genetic studies indicate… 
1998
1998
Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique.
1997
1997
Dideoxy fingerprinting assay for BRCA1 mutation analysis
Since the isolation of BRCA1, the familial breast/ovarian cancer predisposition gene, much effort has been invested in… 
1996
1996
Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasia.
Schmid metaphyseal chondrodysplasia (SMCD; MIM 156500) is an autosomal dominant disorder of the skeleton that is manifested in… 
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