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Prenatal Diagnosis of an Uncommon 48,XX,+18+21 Karyotype in a Fetus With Malformations Typical of Both Trisomies
Prenatal Diagnosis of an Uncommon 48,XX,+18+21 Karyotype in a Fetus With Malformations Typical of Both Trisomies
2020
Patrizia Fiorio
G. Donarini
Ezio Fulcheri
Gabriella Meccariello
Elisa Tassano
Giulia Amico
Dario Paladini
Keywords:
Prenatal diagnosis
Fetus
Karyotype
Obstetrics
Pathology
Medicine
Correction
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