Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations
Objective: We present prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations. Case Report: A 35-year-old, gravida 2, para 1, woman underwent amniocentesis at 17 weeks of gest...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2024-07-01
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| Reeks: | Taiwanese Journal of Obstetrics & Gynecology |
| Onderwerpen: | |
| Online toegang: | http://www.sciencedirect.com/science/article/pii/S1028455924001372 |
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