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Identification of the sequence variations of 15 autosomal STR loci in a Chinese population.

Annals of human biology - 1 Jan 2000

Chen Wenjing, Cheng Jianding, Ou Xueling, Chen Yong, Tong Dayue, Sun Hongyu

Abstract excerpt

BACKGROUND: DNA sequence variation including base(s) changes and insertion or deletion in the primer binding region may cause a null allele and, if this changes the length of the amplified fragment out of the allelic ladder, off-ladder (OL) alleles may be detected. AIM: In order to provide accurate and reliable DNA evidence for forensic DNA analysis, it is essential to clarify sequence variations in prevalently...

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PMID: 24654839
DOI: 10.3109/03014460.2014.897754

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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