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Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation
Among the diseases with X-linked inheritance and intellectual disability, duplication of the Xp11.23p11.22 region is indeed a rare phenomenon, with less than 90 cases known in the literature. Most of them have been recognized with the routine application of array techniques, as these copy number var...
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| Pubblicato in: | Front Genet |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8080037/ https://ncbi.nlm.nih.gov/pubmed/33936165 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.635458 |
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