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Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature
BACKGROUND: Trisomy of the short arm of chromosome 17 is a rare genomic disorder. The clinical features of complete trisomy 17p syndrome have been described. Most cases of this syndrome have been found in infants and children, but only a few cases were found by ultrasound in the prenatal period. MET...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843288/ https://www.ncbi.nlm.nih.gov/pubmed/32951212 http://dx.doi.org/10.1002/jcla.23582 |