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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...
में बचाया:
| में प्रकाशित: | Mol Cell Pediatr |
|---|---|
| मुख्य लेखकों: | , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Springer Berlin Heidelberg
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4530572/ https://ncbi.nlm.nih.gov/pubmed/26542297 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40348-015-0018-2 |
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