Maternal uniparental disomy of chromosome 21 as a cause of pseudo-exclusion from paternity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00438-023-02064-8.pdf
Reference14 articles.
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. https://doi.org/10.1007/s004140050181
2. Cavalheiro CP, Avila E, Gastaldo AZ, Graebin P, Motta CHA, Rodenbusch R, Alho CS (2020) Uniparental disomy of chromosome 21: a statistical approach and application in paternity tests. Forensic Sci Int Genet. https://doi.org/10.1016/j.fsigen.2020.102368
3. Del Gaudio D, Shinawi M, Astbury C, Tayeh MK, Deak KL, Raca G, Laboratory Quality Assurance Committee ACMG (2020) Diagnostic testing for uniparental disomy: a points to consider statement from the American college of medical genetics and genomics (ACMG). Genet Med 22:1133–1141. https://doi.org/10.1038/s41436-020-0782-9
4. Engel E (1980) A new genetic concept: uniparental disomy and its potential effect, isodisomy. Am J Med Genet 6:137–143. https://doi.org/10.1002/ajmg.1320060207
5. Gjertson DW, Brenner CH, Baur MP, Carracedo A, Guidet F, Luque JA, Lessig R, Mayr WR, Pascali VL, Prinz M, Schneider PM, Morling N (2007) ISFG: Recommendations on biostatistics in paternity testing. Forensic Sci Int Genet 1:223–231. https://doi.org/10.1016/j.fsigen.2007.06.006
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