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Methylation-Specific Multiplex Ligation-Dependent Probe Amplification Analysis of Subjects with Chromosome 15 Abnormalities
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are neurodevelopmental disorders caused by loss of expression of imprinted genes from the 15q11-q13 region. They arise from similar defects in the region but differ in parent of origin. There are two recognized typical 15q11-q13 deletions depend...
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| Publicado en: | Genet Test |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2007
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5494700/ https://ncbi.nlm.nih.gov/pubmed/18294067 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gte.2007.0061 |
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