Reinvestigations of six unusual paternity cases by typing of autosomal single-nucleotide polymorphisms

Transfusion

Volumn 52, Issue 2, 2012, Pages 425-430

  Børsting, Claus ^a   Morling, Niels ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOME; DNA FINGERPRINTING; FORENSIC GENETICS; GENE MUTATION; GENETIC MARKER; HUMAN; NUCLEOTIDE SEQUENCE; PATERNITY TEST; SINGLE NUCLEOTIDE POLYMORPHISM;

DNA FINGERPRINTING; FATHERS; FEMALE; GENETIC MARKERS; GENOTYPE; HUMANS; MALE; MICROSATELLITE REPEATS; MOLECULAR TYPING; MOTHERS; PARENT-CHILD RELATIONS; PATERNITY; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84855830274     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/j.1537-2995.2011.03260.x     Document Type: Article

References (20)

1. Thomsen AR, Hallenberg C, Simonsen BT, Langkjær RB, Morling N,. A report of the 2002-2008 paternity testing workshops of the English speaking working group of the International Society of Forensic Genetics. Forensic Sci Int Genet 2009; 3: 214-21.
2. Sanchez JJ, Phillips C, Børsting C, Balogh K, Bogus M, Fondevilla M, Harrison CD, Musgrave-Brown E, Salas A, Syndercombe-Court D, Schneider PM, Carracedo A, Morling N,. A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis 2006; 27: 1713-24.
3. Børsting C, Rockenbauer E, Morling N,. Validation of a single nucleotide polymorphism (SNP) typing assay with 49 SNPs for forensic genetic testing in a laboratory accredited according to the ISO 17025 standard. Forensic Sci Int Genet 2009; 4: 34-42.
4. Børsting C, Sanchez JJ, Hansen HE, Hansen AJ, Bruun HQ, Morling N,. Performance of the SNPforID 52 SNP-plex assay in paternity testing. Forensic Sci Int Genet 2008; 2: 292-300.
5. Porras L, Phillips C, Fondevilla M, Beltrán L, Ortiz T, Rondon F, Barreto G, Lareu MV, Henao J, Carrecedo A,. Genetic variability of the SNPforID 52-plex identification SNP panel in Central West Columbia. Forensic Sci Int Genet 2009; 4: e9-e10.
6. Drobnic K, Børsting C, Rockenbauer E, Tomas C, Morling N,. Typing of 49 autosomal SNPs by SNaPshot® in the Slovenian population. Forensic Sci Int Genet 2010; 4: e125-e127.
7. Santos C, Phillips C, Fondevilla M, Porras-Hurtado L, Carrecedo A, Souto L, Lareu MV,. A study of East Timor variability using the SNPforID 52-plex SNP panel. Forensic Sci Int Genet 2011; 5: e25-e26.
8. Poulsen L, Børsting C, Tomas C, González-Andrade F, Lopez-Pulles R, González-Solõrzano J, Morling N,. Typing of Amerindian Kichwas and Mestizos from Ecuador with the SNPforID multiplex. Forensic Sci Int Genet 2011; 5: e105-7.
9. Amigo J, Phillips C, Lareu MV, Carrecedo A,. The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project. Int J Legal Med 2008; 122: 435-40.
10. Tomas C, Sanchez JJ, Castro JA, Børsting C, Morling N,. Forensic usefulness of a 25 X-chromosome SNP marker set. Transfusion 2010; 50: 2258-65.
11. Børsting C, Morling N,. Mutations and/or relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers. Forensic Sci Int Genet 2011; 5: 236-41.
12. Junge A, Brinkmann B, Fimmers R, Madea B,. Mutations or exclusion: an unusual case in paternity testing. Int J Legal Med 2006; 120: 360-3. (Pubitemid 44630576)
13. González-Andrade F, Sánchez D, Penacino G, Jarreta BM,. Two fathers for the same child: a deficient paternity case of false inclusion with autosomic STRs. Forensic Sci Int Genet 2009; 3: 138-40.
14. Silveira D, Silva FF, Jesus PR, Whittle MR,. Use of X-linked short tandem loci in routine parentage casework. Transfusion 2007; 47: 1050-3. (Pubitemid 46802090)
15. Karlsson AO, Holmlund G, Egeland T, Mostad P,. DNA-testing for immigration cases: the risk of erroneous conclusions. Forensic Sci Int 2007; 172: 144-9. (Pubitemid 47361585)
16. Nothnagel M, Schmidtke J, Krawczak M,. Potentials and limits of pairwise kinship analysis using autosomal short tandem repeat loci. Int J Legal Med 2010; 124: 205-15.
17. Wenk RE, Gjertson DW, Chiafari FA, Houtz T,. The specific power of parentage exclusion in a child's blood relatives. Transfusion 2005; 45: 440-4. (Pubitemid 40389441)
18. Poetsch M, Lüdcke C, Repenning A, Fisher L, Mályusz V, Simeoni E, Lignitz E, Oehmichen M, von Wurmb-Schwark N,. The problem of single parent/child paternity analysis-practical results involving 336 children and 348 unrelated men. Forensic Sci Int 2006; 159: 98-103.
19. Von Wurmb-Schwark N, Mályusz V, Simeoni E, Lignitz E, Poetsch M,. Possible pitfalls in motherless paternity analysis with related putative fathers. Forensic Sci Int 2006; 159: 92-7.
20. Phillips C, Fondevila M, García-Magarinos M, Rodriguez A, Salas A, Carrecedo A, Lareu MV,. Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic Sci Int Genet 2008; 2: 198-204.