Difficulty in genetic counseling of de novo 22q11.2 duplication at amniocentesis and prenatal diagnosis of a 2.9-Mb de novo 22q11.1q11.21 microduplication encompassing TBX1 in a pregnancy associated with no apparently phenotypic abnormality at birth in the fetus

Taiwanese Journal of Obstetrics and Gynecology 2026 Open access

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Authors: Chih-Ping Chen

DOI: 10.1016/j.tjog.2026.03.009

Cited by: 1

References: 17

Fields of Study & Subjects

Congenital heart defects research Prenatal Screening and Diagnostics Williams Syndrome Research

References 17