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A case of polimalformed fetus with a microdeletion of CTNNA3 gene
We report a case of a male fetus of 20 weeks of gestation with plurimalformed observed by transonic scan and confirmed by MR. The karyotype was 46, XY. Molecular analysis showed a microdeletion of about 100 kb in the CTNNA3 gene.
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| Publicat a: | J Prenat Med |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
CIC Edizioni Internazionali
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5505477/ https://ncbi.nlm.nih.gov/pubmed/28725342 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/jpm/2016.10.3.020 |
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