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Literature DB >> 16604363

Mother-child exclusion due to paternal uniparental disomy 6.

R Wegener¹, V Weirich, E M Dauber, W R Mayr.

Abstract

In a mother-child pair, false exclusions in markers on chromosome 6 have been observed. The genetic incompatibilities have been caused by paternal uniparental disomy. The consequences of such cases for investigations of parentage are discussed.

Entities: Disease Species

Mesh：

Year: 2006 PMID： 16604363 DOI： 10.1007/s00414-006-0077-y

Source DB: PubMed Journal: Int J Legal Med ISSN： 0937-9827 Impact factor: 2.686

14 in total

1. Disputed maternity leading to identification of tetragametic chimerism.

Authors: Neng Yu; Margot S Kruskall; Juan J Yunis; Joan H M Knoll; Lynne Uhl; Sharon Alosco; Marina Ohashi; Olga Clavijo; Zaheed Husain; Emilio J Yunis; Jorge J Yunis; Edmond J Yunis
Journal: N Engl J Med Date: 2002-05-16 Impact factor: 91.245

2. Population genetics of the 15 AmpF lSTR Identifiler loci in Kosovo Albanians.

Authors: M Kubat; J Skavić; I Behluli; B Nuraj; T Bekteshi; M Behluli; I Martinović Klarić; M Pericić
Journal: Int J Legal Med Date: 2004-01-23 Impact factor: 2.686

3. Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region.

Authors: Marielle Heinrich; Miriam Müller; Steven Rand; Bernd Brinkmann; Carsten Hohoff
Journal: Int J Legal Med Date: 2004-08-20 Impact factor: 2.686

4. Bosnian population data for the 15 STR loci in the Power Plex 16 kit.

Authors: R Konjhodzić; M Kubat; J Skavić
Journal: Int J Legal Med Date: 2004-02-28 Impact factor: 2.686

5. ACTBP2 (alias ACTBP8) is localized on chromosome 6 (band 6q14).

Authors: S Wenda; E M Dauber; D W M Schwartz; C Jungbauer; V Weirich; R Wegener; W R Mayr
Journal: Forensic Sci Int Date: 2005-03-10 Impact factor: 2.395

6. Tetranucleotide repeat polymorphism at the human beta-actin related pseudogene H-beta-Ac-psi-2 (ACTBP2).

Authors: M H Polymeropoulos; D S Rath; H Xiao; C R Merril
Journal: Nucleic Acids Res Date: 1992-03-25 Impact factor: 16.971

7. Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat.

Authors: B Brinkmann; M Klintschar; F Neuhuber; J Hühne; B Rolf
Journal: Am J Hum Genet Date: 1998-06 Impact factor: 11.025

8. DNA typing in cases of blood chimerism.

Authors: A Milde; R Kühl-Burmeister; S Ritz-Timme; H J Kaatsch
Journal: Int J Legal Med Date: 1999 Impact factor: 2.686

9. Pseudo-exclusion from paternity due to maternal uniparental disomy 16.

Authors: G Bein; B Driller; M Schürmann; P M Schneider; H Kirchner
Journal: Int J Legal Med Date: 1998 Impact factor: 2.686

10. A new genetic concept: uniparental disomy and its potential effect, isodisomy.

Authors: E Engel
Journal: Am J Med Genet Date: 1980

3 in total

1. Haplotype-assisted characterization of germline mutations at short tandem repeat loci.

Authors: Miriam Müller; Ulla Sibbing; Carsten Hohoff; Bernd Brinkmann
Journal: Int J Legal Med Date: 2009-11-11 Impact factor: 2.686

2. One person with two DNA profiles: a(nother) case of mosaicism or chimerism.

Authors: Vincent Castella; Maria del Mar Lesta; Patrice Mangin
Journal: Int J Legal Med Date: 2009-02-25 Impact factor: 2.686

3. Maternal uniparental isodisomy for chromosome 6 discovered by paternity testing: a case report.

Authors: Elizabeth R Kerr; Gary M Stuhlmiller; George C Maha; Mark A Ladd; Fady M Mikhail; Ruth P Koester; Anna C E Hurst
Journal: Mol Cytogenet Date: 2018-12-20 Impact factor: 2.009

3 in total