Mother-child exclusion due to paternal uniparental disomy 6

International Journal of Legal Medicine

Volumn 120, Issue 5, 2006, Pages 282-285

  Wegener, R ^a   Weirich, V ^a   Dauber, E M ^b   Mayr, W R ^b  

^a UNIVERSITY OF ROSTOCK   (Germany)

^b MEDICAL UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHIMERA; CHROMOSOME 6; FEMALE; GENE LOCUS; GENETIC INCOMPATIBILITY; GENOTYPE; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; KARYOTYPE 46,XX; MALE; MOTHER; MUTATION; NULL ALLELE; PATERNITY TEST; PHENOTYPE; PRIORITY JOURNAL; SHORT TANDEM REPEAT; UNIPARENTAL DISOMY; X CHROMOSOME;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; HUMANS; MALE; PATERNITY; UNIPARENTAL DISOMY;

EID: 33747356776     PISSN: 09379827     EISSN: 14371596     Source Type: Journal    
DOI: 10.1007/s00414-006-0077-y     Document Type: Article

References (16)

1. Bein G, Driller B, Schürmann M, Schneider PM, Kirchner H (1998) Pseudo-exclusion from paternity due to maternal uniparental disomy 16. Int J Legal Med 111:328-330
2. Brinkmann B, Klintschar M, Neuhuber F, Hühne J, Rolf B (1998) Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am J Hum Genet 62:1408-1415
3. Brinkmann B, Pfeiffer H, Schürenkamp M, Hohoff C (2001) The evidential value of STRs. An analysis of exclusion cases. Int J Legal Med 114:173-177
4. Dauber EM, Glock B, Mayr D, Mayr WR (1999) A case of dispermic chimerism: importance of DNA polymorphisms. J Biol Regul Homeost Agents 13:51-53
5. Engel E (1980) A new genetic concept: uniparental disomy and its potential effect, isodisomy. Am J Med Genet 6:137-143
6. Engel E, Antonarakis SE (2002) Genomic imprinting and uniparental disomy in medicine. Wiley-Liss, New York, NY, USA
7. Gunzer C, Dauber EM, Petrasek M, Glock B, Schwartz DWM, Mayr WR (2004) Apparent exclusion of maternity in a twin chimera carrying only her twin brother's blood cells. Vox Sang 87[Suppl 3]:130
8. Heinrich M, Müller M, Rand S, Brinkmann B, Hohoff C (2004) Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region. Int J Legal Med 118:361-363
9. Konjhodzic R, Kubat M, Skavic J (2004) Bosnian population data for the 15 STR loci in the Power Plex 16 kit. Int J Legal Med 118:119-121
10. Kubat M, Skavic J, Behluli I, Nuraj B, Bekteshi T, Behluli M, Martinovic Klaric I, Pericic M (2004) Population genetics of the 15 AmpFlSTR Identifiler loci in Kosovo Albanians. Int J Legal Med 118:115-118
11. Mayr WR (1981) Human chimerism. Rev Fr Transfus Immunohematol 24:19-26
12. Mayr WR, Pausch V, Schnedl W (1979) Human chimera detectable only by investigation of her progeny. Nature 277:210-211
13. Milde A, Kühl-Burmeister R, Ritz-Timme S, Kaatsch HJ (1999) DNA typing in cases of blood chimerism. Int J Legal Med 112:333-335
14. Polymeropoulos MH, Rath DS, Xiao H, Merril CR (1992) Tetranucleotide repeat polymorphism at the human beta-actin related pseudogene H-beta-Ac-psi-2 (ACTBP2). Nucleic Acids Res 20:1432
15. Wenda S, Dauber EM, Schwartz DWM, Jungbauer C, Weirich V, Wegener R, Mayr WR (2005) ACTBP2 (alias ACTBP8) is localized on chromosome 6 (band 6q14). Forensic Sci Int 148:207-209
16. Yu N, Kruskall MS, Yunis JJ, Knoll JHM, Uhl L, Alsoco S, Ohashi M, Clavijo O, Husain Z, Yunis EJ, Yunis JJ, Yunis EJ (2002) Disputed maternity leading to the identification of tetragametic chimerism. N Engl J Med 346:1545-1552