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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Egile Nagusiak: Chih-Ping Chen (Egilea), Fang-Tzu Wu (Egilea), Yen-Ting Pan (Egilea), Peih-Shan Wu (Egilea), Meng-Shan Lee (Egilea), Wayseen Wang (Egilea)
Formatua: Liburua
Argitaratua: Elsevier, 2024-07-01T00:00:00Z.
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