« Previous
Next »
Forensic Science International: Genetics
Volume 1, Issue 2
, Pages 93-99
, June 2007
X-chromosomal markers: Past, present and future
References
- . The Xg blood group system: a review. Transfus. Med. Rev. 1998;12(4):233–257
- . Tetranucleotide repeat polymorphism at the HPRT locus. Nucleic Acids Res. 1991;19(19):5450
- . Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics. 1992;12(2):241–253
- . Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA). J. Forensic Sci. 1998;43(5):1046–1049
- . Duplex PCR of the Y-27H39 and HPRT loci with reference to Japanese population data on the HPRT locus. Nippon Hoigaku Zasshi. 1997;51(2):67–69
- . On the utilization of erythrocyte acid phosphatase polymorphism in paternity evaluation. Dtsch. Z. Gesamte Gerichtl. Med. 1968;64(2):127–146
- . Use of X-linked markers for forensic purposes. Int. J. Legal Med. 2003;117(2):67–74
- . Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961;190:372–373
- . The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Hum. Mol. Genet. 2000;9(5):695–702
- . Clinical and molecular aspects of androgen receptor defects. Exp. Clin. Endocrinol. Diabetes. 1998;106(6):446–453
- . Pseudo-exclusion from paternity due to maternal uniparental disomy 16. Int. J. Legal Med. 1998;111(6):328–330
- . Mother–child exclusion due to paternal uniparental disomy 6. Int. J. Legal Med. 2006;120:282–285
- . Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J. Clin. Endocrinol. Metab. 2003;88(2):622–626
- Evaluation of Y-chromosomal STRs: a multicenter study. Int. J. Legal Med. 1997;110(3):125–133141–129
- . Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts. Hum. Genet. 1992;89(4):389–394
- . A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci. Hum. Mol. Genet. 1993;2(4):431–437
- . The HumARA genotype is linked to spinal and bulbar muscular dystrophy and some further disease risks and should no longer be used as a DNA marker for forensic purposes. Int. J. Legal Med. 2005;119(3):179–180
- . Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature. 1991;352(6330):77–79
- . DXS10011: studies on structure, allele distribution in three populations and genetic linkage to further q-telomeric chromosome X markers. Int. J. Legal Med. 2004;118(6):313–319
- . MiniX-STR multiplex system population study in Japan and application to degraded DNA analysis. Int. J. Legal Med. 2006;1–8
- . Prenatal exclusion without involving the putative fathers of an incestuous father–daughter parenthood. Prenat. Diagn. 2004;24(8):662–664
- . DXS10079, DXS10074 and DXS10075 are STRs located within a 280-kb region of Xq12 and provide stable haplotypes useful for complex kinship cases. Int. J. Legal Med. 2005;1–9
- H. Rodig, F. Kloep, L. Weißbach, C. Augustin, J. Edelmann, S. Hering, R. Szibor, F. Götz, W. Brabetz, Evaluation of 7 X-chromosomal Short Tandem Repeat loci located within the Xq26 region, in press.
- . Validation of the STR DXS7424 and the linkage situation on the X-chromosome. Forensic Sci. Int. 2002;125:217–222
- . Haplotyping of STR cluster DXS6801–DXS6809–DXS6789 on Xq21 provides a powerful tool for kinship testing. Int. J. Legal Med. 2005;119(6):363–369
- . Forensic evaluation of three closely linked STR markers in a 13kb region at Xp11.23. Int. Congress Ser. 2006;1239:311–314
- . Study of six X-linked tetranucleotide microsatellites: population data from five Spanish regions. Int. J. Legal Med. 2005;1–4
- . Genetic analysis of 18 X-linked short tandem repeat markers in Korean population. Forensic Sci. Int. 2005;147(1):35–41
- . Development of a pentaplex X-chromosomal short tandem repeat typing system and population genetic studies. Forensic Sci. Int. 2005;154(2/3):173–180
- . Linkage disequilibrium in the human genome. Nature. 2001;411(6834):199–204
- . Using mitochondrial and nuclear DNA markers to reconstruct human evolution. Bioessays. 1998;20(2):126–136
- . Extensive linkage disequilibrium in small human populations in Eurasia. Am. J. Hum. Genet. 2002;70(3):673–685
- . Validation of the HumDXS6807 short tandem repeat polymorphism for forensic application. Electrophoresis. 1999;20(14):2844–2846
- . 16 X-chromosome STR loci frequency data from a German population. Forensic Sci. Int. 2001;124(2/3):215–218
- . Development of the X-linked tetrameric microsatellite marker DXS9898 for forensic purposes. J. Forensic Sci. 2000;45(4):929–931
- . Validation of the X-linked STR DXS6801. Forensic Sci. Int. 2005;148:219–220
- . Validation of the X-chromosomal STR DXS6809. Int. J. Legal Med. 2003;117(4):241–244
- . Development of the X-linked tetrameric microsatellite marker HumDXS6789 for forensic purposes. Forensic Sci. Int. 2001;119(1):42–46
- . DXS101: a highly polymorphic X-linked STR. Int. J. Legal Med. 2001;114(4/5):301–304
- . DXS6797 contains two STRs which can be easily haplotyped in both sexes. Int. J. Legal Med. 2006;120(2):61–66
- . Development of two pentaplex systems with X-chromosomal STR loci and their allele frequencies in a northeast German population. Forensic Sci. Int. 2005;155(1):71–76
- . Forensic validation of the X-chromosomal STR-markers GATA165B12, GATA164A09, DXS9908 and DXS7127 in German population. Int. Congress Ser. 2006;1239:298–300
- . Sequence structure and population data of the X-linked markers DXS7423 and DXS8377—clarification of conflicting statements published by two working groups. Forensic Sci. Int. 2003;134(1):72–73
PII: S1872-4973(07)00069-5
doi: 10.1016/j.fsigen.2007.03.003
© 2007 Elsevier Ireland Ltd. All rights reserved.
« Previous
Next »
Forensic Science International: Genetics
Volume 1, Issue 2
, Pages 93-99
, June 2007
