Evaluation of seven X-chromosomal short tandem repeat loci located within the Xq26 region-Reference-Cited by-同舟云学术

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Evaluation of seven X-chromosomal short tandem repeat loci located within the Xq26 region

Published:2010-04 Issue:3 Volume:4 Page:194-199
ISSN:1872-4973
Container-title:Forensic Science International: Genetics
language:en
Short-container-title:Forensic Science International: Genetics

Author:

Rodig Heike,Kloep Frank,Weißbach Lydia,Augustin Christa,Edelmann Jeannett,Hering Sandra,Szibor Reinhard,Götz Frank,Brabetz Werner

Publisher

Elsevier BV

Subject

Genetics,Pathology and Forensic Medicine

Reference23 articles.

1. Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA);Desmarais;J. Forensic Sci.,1998

2. Validation of the STR DXS7424 and the linkage situation on the X-chromosome;Edelmann;Forensic Sci. Int.,2002

3. Use of X-linked markers for forensic purposes;Szibor;Int. J. Legal Med.,2003

4. Haplotyping of STR cluster DXS6801-DXS6809-DXS6789 on Xq21 provides a powerful tool for kinship testing;Szibor;Int. J. Legal Med.,2005

5. DXS10079, DXS10074 and DXS10075 are STRs located within a 280kb region at Xq12 and provide stable haplotypes useful in the solving of complex kinship cases;Hering;Int. J. Legal Med.,2006

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1. Construction of 13-locus X-STR multiplex PCR system that reinforces Argus X-12 kit discrimination capacity: Application to the Malay population;Legal Medicine;2024-09

2. X-chromosome short tandem repeats (X-STRs): Applications for human remains identification;Forensic Genetic Approaches for Identification of Human Skeletal Remains;2023

3. Development and validation of a new 18 X‐STR typing assay for forensic applications;ELECTROPHORESIS;2021-01-27

4. Genetic polymorphism of 27 X-chromosomal short tandem repeats in an Egyptian population;Legal Medicine;2019-03

5. A simple method for calculating the likelihood ratio in a kinship test using X-chromosomal markers incorporating linkage, linkage disequilibrium, and mutation;Legal Medicine;2018-05

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