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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104164/ https://www.ncbi.nlm.nih.gov/pubmed/33538077 http://dx.doi.org/10.1002/mgg3.1605 |