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Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype
Trisomy 3q is a very rarely reported chromosomal disorder. Duplication of part of the long arm of human chromosome 3 causes a distinct and severe syndrome that leads to multiple congenital abnormalities. A 27 year-old pregnant woman was admitted to our clinic at 17 weeks of gestation. Prenatal sonog...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
AVES
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3939159/ https://ncbi.nlm.nih.gov/pubmed/24591944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/jtgga.2010.45 |
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