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Submicroscopic copy-number variations associated with 46,XY disorders of sex development
BACKGROUND: Mutations in known causative genes and cytogenetically detectable chromosomal rearrangements account for a fraction of cases with 46,XY disorders of sex development (DSD). Recent advances in molecular cytogenetic technologies, including array-based comparative genomic hybridization (aCGH...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Berlin Heidelberg
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530572/ https://www.ncbi.nlm.nih.gov/pubmed/26542297 http://dx.doi.org/10.1186/s40348-015-0018-2 |