Molecular cytogenetics of Prader-Willi and Angelman syndromes
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference2 articles.
1. Parental origin of chromosome 15 deletion in Prader-Willi syndrome;Butler;Lancet,1983
2. Angelman and Prader-Willi syndrome share a common chromosome 15 deletion, but differ in parental origin of the deletion;Knoll;Am J Med Genet,1989
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Chromosome Heteromorphism (Summaries);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017
2. Chromosome 15;Human Chromosome Variation: Heteromorphism and Polymorphism;2011
3. Plates;Atlas of Human Chromosome Heteromorphisms;2004
4. High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome;American Journal of Medical Genetics;1995-05-08
5. Are specific short arm variants or heteromorphisms over-represented in the chromosome 15 deletion in Angelman or Prader-Willi syndrome patients?;American Journal of Medical Genetics;1994-03-01
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