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Delineation variable genotype/phenotype correlations of 6q27 terminal deletion derived from dic(6;18)(q27;p10)
BACKGROUND: Terminal deletion of 6q27 produces a rare syndrome associated with unexplained mental retardation, hypotonia, epilepsy, and multiple malformations. Structural brain malformations are consistently observed, including agenesis of the corpus callosum, hydrocephalus, periventricular nodular...
Autores principales: | Zhou, Lili, Chen, Chong, Li, Huanzheng, Chen, Yunying, Xu, Xueqin, Lin, Xiaoling, Tang, Shaohua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243269/ https://www.ncbi.nlm.nih.gov/pubmed/25426168 http://dx.doi.org/10.1186/s13039-014-0078-3 |
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