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Clinical and molecular characterization of a de novo 19p13.3 microdeletion
BACKGROUND: Structural rearrangements of chromosome 19p13.3 are a rare condition, and their phenotypic consequences remain not well defined, because of the variability of clinical manifestations. Increasing knowledge of new 19p13.3 microdeletion is useful to clarify the phenotypic variability observ...
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| Publicat a: | Mol Cytogenet |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4882821/ https://ncbi.nlm.nih.gov/pubmed/27239227 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-016-0252-x |
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