Results 191 to 200 of about 29,344 (206)
Some of the next articles are maybe not open access.

Bioassay of kinship using VNTR alleles

1994
Much attention has been given to forensic statistics. Focus has been on matching criteria, on binning procedures and likelihood ratios, and on VNTR genotype distribution in forensic populations (e.g. Lander 1989, Cohen 1990, Chakraborty 1991, Lewontin and Hartl 1991, Evett and Pinchin 1991, Nichols and Balding, 1991). Newton Morton deserves much credit
Bjørnar Olaisen   +2 more
openaire   +1 more source

VNTR: Application to prenatal diagnosis

2019
Purpose: In prenatal diagnosis maternal DNA contamination of the CVS (chorionic villus sample) must be excluded for obtaining reliable results. The purpose of this was to study three VNTR (variable number of tandem repeats) loci by PCR for the elimination of the maternal DNA contamination in CVSs.
Attila G.   +6 more
openaire   +1 more source

VNTRs

2022
openaire   +1 more source

VNTR at the DXYS14 locus

Human Molecular Genetics, 1994
M G, Le Roux   +5 more
openaire   +2 more sources

VNTR

2008
openaire   +1 more source

Monoclonal Antibodies to Mucin VNTR Peptides

2000
P X, Xing   +3 more
openaire   +2 more sources

A new VNTR polymorphism at locus D1S340

Human Molecular Genetics, 1993
M, Honma   +6 more
openaire   +2 more sources

[VNTR and transcription regulator].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 1998
K, Koyama, Y, Nakamura
openaire   +1 more source

Home - About - Disclaimer - Privacy