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MR Imaging Findings in Xp21.2 Duplication Syndrome
Xp21.2 duplication syndrome is a rare genetic disorder of undetermined prevalence and clinical relevance. As the use of chromosomal microarray has become first line for the work-up of childhood developmental delay, more gene deletions and duplications have been recognized. To the best of our knowled...
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| Pubblicato in: | J Radiol Case Rep |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
EduRad
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5065289/ https://ncbi.nlm.nih.gov/pubmed/27761175 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3941/jrcr.v10i5.2563 |
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