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Noninvasive prenatal testing aids identification of tetrasomy 18p: A case report
Tetrasomy 18p syndrome (Online Mendelian Inheritance in Man 614290) is a rare chromosomal disorder that is seen in approximately 1 in every 180,000 live births. It is caused by the presence of isochromosome 18p, which is a supernumerary marker composed of two copies of the short arms of chromosome 1...
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| Publicado no: | Case Rep Womens Health |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7334301/ https://ncbi.nlm.nih.gov/pubmed/32642449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.crwh.2020.e00236 |
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