Non-chromosome 15 marker chromosome in a Prader-Willi syndrome patient with uniparental disomy
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2006.02163.x/fullpdf
Reference9 articles.
1. Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes
2. Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
3. FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patients
4. Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations
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1. Complex and segmental uniparental disomy updated;Journal of Medical Genetics;2008-06-04
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