Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case
Author:
Funder
National Natural Science Foundation of China
CAS Key Program
Publisher
Springer Science and Business Media LLC
Subject
Pathology and Forensic Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00414-018-1857-x.pdf
Reference15 articles.
1. Robinson WP (2000) Mechanisms leading to uniparental disomy and their clinical consequences. BioEssays 22:452–459. https://doi.org/10.1002/(sici)1521-1878(200005)22:5<452::aid-bies7>3.0.co;2-k
2. Liehr T (2010) Cytogenetic contribution to uniparental disomy (UPD). Mol Cytogenet 3:8. https://doi.org/10.1186/1755-8166-3-8
3. Wegener R, Weirich V, Dauber EM, Mayr WR (2006) Mother-child exclusion due to paternal uniparental disomy 6. Int J Legal Med 120:282–285. https://doi.org/10.1007/s00414-006-0077-y
4. Mansuet-Lupo A, Henke J, Henke L, Blank C, Ernsting A, Kozlowski P, Rouger P, van Huffel V (2009) A paternity case with three genetic incompatibilities between father and child due to maternal uniparental disomy 21 and a mutation at the Y chromosome. Forensic Sci Int Genet 3:141–143. https://doi.org/10.1016/j.fsigen.2008.09.010
5. Heide E, Heide KG, Rodewald A (2000) Maternal uniparental disomy (UPD) for chromosome 2 discovered by exclusion of paternity. Am J Med Genet 92:260–263
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