SOLVED: Markers: D3S1358, vWA, D165539, CSFIPO, TPOX, D8S1179, D21S11, D18S51, D2S441, D19S433, THO1, FGA, D22S1045, D5S818, D135317, D7S820, SE33, 010S1248, D1S1656, D125391, D2S1338 Child Alleged Father Mother Paternity Index: 15, 1.5674, 16,
A case of tri-allelic pattern at locus D3S1358 on chromosome 3p21 inherited from paternal grandmother - ScienceDirect
Solved Part A. Use this information to calculate the | Chegg.com
Comparison of human DNA profiles with loci D3S1358, THO1, D21S11,... | Download Scientific Diagram
A depiction of the D3S1358 locus showing a two-person profile.... | Download Scientific Diagram
Schematic representation of library preparation and NGS. Data for... | Download Scientific Diagram
MIX05 Case 1 mixture results at the D3S1358 locus from five different... | Download Scientific Diagram
SOLVED: 08. Genetic Diversity and Sexual Reproduction: Calculate how many genotypes would be possible among the children of Bob and Anne for the combined DNA profile from the D3S1358, vWA, and FGA.
Observed single-step mutation in D3S1358 locus . | Download Scientific Diagram
Physical location and linked genes of common forensic STR markers
Locus Child D3S1358 Alleged Father 15, 19 15, 23 12, | Chegg.com
Analysis of STR DNA Loci
Forensic Applications of Next Generation Sequencing | NIST
A Single Step Mutation at D3S1358 Locus in a DNA Paternity Testing with 2 Alleged Fathers. | Semantic Scholar
What does d3s1358 mean on a DNA test?
GENOTYPES OF PATIENT 1 Locus D3S1358 VWA FGA | Download Table
Discordance at D3S1358 locus involving SGM Plus™ and the European new generation multiplex kits. | Semantic Scholar
a–c Representative images of microsatellite-based deletion analysis of... | Download Scientific Diagram
Solved Locus Locus Locus Allele Frequency D3S1358 12 0.015 | Chegg.com
Green dye channel of AmpFISTR Identifiler kit containing the D3S1358... | Download Scientific Diagram
The figure illustrates the results of an | Chegg.com
Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations | Chinese Medical Journal
