Maternal uniparental isodisomy for chromosome 6 discovered by paternity testing: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Link
http://link.springer.com/content/pdf/10.1186/s13039-018-0411-3.pdf
Reference12 articles.
1. Engel E. A new genetic concept: uniparental disomy and its potential effect, isodisomy. Am J Med Genet. 1980;6:137–43.
2. Yamazawa K, Ogata T, Ferguson-Smith AC. Uniparental disomy and human disease: an overview. Am J Med Genet Part C Semin Med Genet. 2010;154C:329–34.
3. Siegel DH, Slavotinek A. Uniparental Disomy. Pediatr Dermatol. 2005;22(5):482–7.
4. Bein G, Driller B, Shürmann M, Schneider PM, Kirchner H. Pseudo-exclusion from paternity due to maternal uniparental disomy 16. Int J Legal Med. 1998;111:328–30.
5. Heide E, Heide KG, Rodewald A. Maternal uniparental disomy (UPD) for chromosome 2 discovered by exclusion of paternity. Am J Med Genet. 2000;92:260–3.
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