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Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome
BACKGROUND: Several studies have reported on the clinical phenotype of the 17q12 microduplication syndrome, a rare autosomal dominant genetic disorder, in children and adults, but few have reported on its prenatal diagnosis. This study analyzed the prenatal ultrasound phenotypes of the 17q12 microdu...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399630/ https://www.ncbi.nlm.nih.gov/pubmed/36034547 http://dx.doi.org/10.3389/fped.2022.910497 |