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Ultrasonographic findings and prenatal diagnosis of Jacobsen syndrome: A case report and review of the literature
RATIONALE: Jacobsen syndrome (JBS) is a rare chromosomal disorder with variable phenotypic expressivity, which is usually diagnosed in infancy and childhood based on clinical examination and hematological and cytogenetic findings. Prenatal diagnosis and fetal ultrasonographic findings of JBS are rar...
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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6946260/ https://ncbi.nlm.nih.gov/pubmed/31895838 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000018695 |
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