The structure of a variant allele which is considered to be 30.3 in the STR locus D21S11

Legal Medicine

Volumn 8, Issue 3, 2006, Pages 182-183

  Tsuji, Akiko ^a   Ishiko, Atsushi ^a,b   Ikeda, Noriaki ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b Forensic Science Laboratory   (Japan)

Author keywords

D21S11; Sequence structure; Variant allele

Indexed keywords

ADULT; ALLELE; ARTICLE; DNA SEQUENCE; FEMALE; HUMAN; MALE; MEDICAL RESEARCH; NEWBORN; PATERNITY TEST; SEQUENCE ANALYSIS; SHORT TANDEM REPEAT;

ADULT; ALLELES; BASE SEQUENCE; FEMALE; GENETIC VARIATION; HUMANS; INFANT, NEWBORN; MALE; PATERNITY; TANDEM REPEAT SEQUENCES; VARIATION (GENETICS);

EID: 33747206840     PISSN: 13446223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.legalmed.2005.12.001     Document Type: Article

References (3)

1. Zhou H.-G., Sato K., Nishimaki Y., Fang L., and Hasekura H. The HumD21S11 system of short tandem repeat DNA polymorphisms in Japanese and Chinese. Forensic Sci Int 86 (1997) 109-118
2. Thangaraj K., Reddy A.G., and Singh L. Mutation in the STR locus D21S11 of father causing allele mismatch in the child. J Forensic Sci 49 (2004) 99-103
3. Moller A., Meyer E., and Brinkmann B. Different types of structural variation in STRs: HumFES/FPS, HumVWA and HumD21S11. Int J Legal Med 106 (1994) 319-323