Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother
Objective: We present prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother. Case report: A 28-year-old woman primigravid underwent amniocentesis at 23 weeks of gestation because of fetal ultrasoun...
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| Materiálatiipa: | Girji |
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Elsevier,
2021-01-01T00:00:00Z.
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A1234.567 |
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