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Deletion of Chromosome 13 due to Different Rearrangements and Impact on Phenotype
Patients with deletion of chromosome 13 present with variable clinical features, and the correlation between phenotype and genomic aberration is not well established in the literature, mainly due to variable sizes of the deleted segments and inaccuracy of breakpoint mapping. In order to improve the...
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| Publicado no: | Mol Syndromol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6528091/ https://ncbi.nlm.nih.gov/pubmed/31191202 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000497402 |
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