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Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
BACKGROUND: While Miller-Dieker syndrome critical region deletions are well known delineated anomalies, submicroscopic duplications in this region have recently emerged as a new distinctive syndrome. So far, only few cases have been described overlapping 17p13.3 duplications. METHODS: In this study,...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006381/ https://www.ncbi.nlm.nih.gov/pubmed/32028920 http://dx.doi.org/10.1186/s12881-020-0966-9 |