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A report on seven fetal cases associated with 15q11‐q13 microdeletion and microduplication
BACKGROUND: The 15q11‐q13 region contains three breakpoints (BP1 to BP3), and copy number variations often occur in the region. AIMS: 15q11‐q13 microdeletion and microduplication are usually associated with Prader‐Willi and Angelman syndromes, respectively. It is not yet clear to what extent microde...
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| Publicado en: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8104164/ https://ncbi.nlm.nih.gov/pubmed/33538077 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1605 |
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