Molecular characterization of a null allele at locus DXS8378

Forensic Science International: Genetics Supplement Series

Volumn 1, Issue 1, 2008, Pages 160-161

  Robino, C ^a   Inturri, S ^a   Varacalli, S ^a   Piccinini, A ^b   Gino, S ^a   Torre, C ^a  

^a UNIVERSITY OF TURIN   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

DXS8378; Null allele; Paternity testing; Short tandem repeat; X chromosome

Indexed keywords

ARTICLE; CONTROLLED STUDY; FEMALE; GENE AMPLIFICATION; GENE LOCUS; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; NORMAL HUMAN; NUCLEOTIDE SEQUENCE; NULL ALLELE; PATERNITY TEST; POINT MUTATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SHORT TANDEM REPEAT; X CHROMOSOME;

EID: 50349096675     PISSN: 18751768     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fsigss.2007.10.124     Document Type: Article

References (4)

1. Robino C., Giolitti A., Gino S., and Torre C. Development of two multiplex PCR systems for the analysis of 12 X-chromosomal STR loci in a northwestern Italian population sample. Int. J. Legal Med. 120 (2006) 315-318
2. Edelmann J., Deichsel D., Hering S., Plate I., and Szibor R. Sequence variation and allele nomenclature for the X-linked STRs DXS9895, DXS8378, DXS7132, DXS6800, DXS7133, GATA172D05, DXS7423 and DXS8377. Forensic Sci. Int. 129 (2002) 99-103
3. Ross M.T., Grafham D.V., Coffey A.J., et al. The DNA sequence of the human X chromosome. Nature 434 (2005) 325-337
4. Gomes I., Prinz M., Pereira R., et al. Genetic analysis of three US population groups using an X-chromosomal STR decaplex. Int. J. Legal Med. 121 (2007) 198-203